Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2004-001317-34 | EudraCT Number | EudraCT |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
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A phase III, randomised, parallel-group, double-blind, active controlled study to investigate the ef ficacy and safety of two different dose regimens of orally administered dabigatran etexilate capsule s [150 or 220 mg once daily starting with a half dose (i.e.75 or 110 mg) on the day of surgery] comp ared to subcutaneous enoxaparin 40 mg once daily for 6 to 10 days, in prevention of venous thromboem bolism in patients with primary elective total knee replacement surgery. RE-MODEL (Thromboembolism prevention after knee surgery)
Not provided
Not provided
Not provided
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| dabigatran etexilate 220 mg | Experimental | 220 mg once daily |
|
| dabigatran etexilate 150 mg | Experimental | 150 mg once daily |
|
| enoxaparin | Active Comparator | 40 mg once daily |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| enoxaparin | Drug | 40 mg once daily |
| |
| dabigatran etexilate |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Total Venous Thromboembolic Event and All-cause Mortality During Treatment Period | Total Venous Thromboembolic Event (VTE) includes both proximal and distal deep vein thrombosis (DVT) (detected by routine bilateral venography), symptomatic DVT (confirmed by venous compression ultrasound, venography or autopsy) and pulmonary embolism (PE) (confirmed by pulmonary V-Q scintigraphy, chest x-ray, pulmonary angiography, spiral CT or autopsy). All of these components and all deaths were centrally adjudicated by the VTE events committee, which was not aware of the treatment allocation of the patients. | First administration until 6-10 days |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Major Venous Thromboembolic Event and Venous Thromboembolic Event-related Mortality During Treatment Period | Major Venous Thromboembolic Event (VTE) is defined as proximal DVT and PE, as adjudicated by the VTE events committee | First administration until 6-10 days |
| Number of Participants With Proximal Deep Vein Thrombosis During Treatment Period |
Not provided
Inclusion criteria
Inclusion criteria (selected):
Exclusion criteria
Exclusion criteria (selected):
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Boehringer Ingelheim | Boehringer Ingelheim | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| 1160.25.06108 Boehringer Ingelheim Investigational Site | Garren | Australian Capital Territory | Australia | |||
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22995531 | Derived | Eriksson BI, Dahl OE, Rosencher N, Clemens A, Hantel S, Kurth AA. Efficacy of delayed thromboprophylaxis with dabigatran: pooled analysis. Thromb Res. 2012 Dec;130(6):871-6. doi: 10.1016/j.thromres.2012.08.315. Epub 2012 Sep 17. | |
| 22709460 | Derived | Rosencher N, Noack H, Feuring M, Clemens A, Friedman RJ, Eriksson BI. Type of anaesthesia and the safety and efficacy of thromboprophylaxis with enoxaparin or dabigatran etexilate in major orthopaedic surgery: pooled analysis of three randomized controlled trials. Thromb J. 2012 Jun 18;10(1):9. doi: 10.1186/1477-9560-10-9. |
Not provided
Not provided
Whilst 2101 patients were enrolled/randomised to treatment prior to surgery in this trial, only 2076 started treatment. Therefore, 25 patients were randomised but not treated (treatment was planned to start post surgery).
The treatment period is from first administration of study medication, until 3 days after last administration of study medication. Treatment duration is planned for 8 days. The study period is from first administration of study medication until day 84 - 91.
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | Dabigatran 220mg | qd (once daily) oral |
| FG001 | Dabigatran 150mg | qd (once daily) oral |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Drug |
150 mg once daily |
|
| dabigatran etexilate | Drug | 220 mg once daily |
|
Proximal Deep Vein Thrombosis as adjudicated by the VTE events committee |
| First administration until 6-10 days |
| Number of Participants With Total Deep Vein Thrombosis During Treatment Period | Total Deep Vein Thrombosis as adjudicated by the VTE events committee | First administration until 6-10 days |
| Number of Participants With Symptomatic Deep Vein Thrombosis During Treatment Period | Symptomatic Deep Vein Thrombosis, confirmed by venous compression ultrasound, venography or autopsy, and as adjudicated by the VTE events committee | First administration until 6-10 days |
| Number of Participants With Pulmonary Embolism During Treatment Period | Pulmonary embolism confirmed by pulmonary V-Q scintigraphy, chest x-ray, pulmonary angiography, spiral CT or autopsy, and as adjudicated by the VTE events committee | First administration until 6-10 days |
| Number of Participants Who Died During Treatment Period | All cause death, as adjudicated by the VTE events committee | First administration until 6-10 days |
| Number of Participants With Total Venous Thromboembolic Event (VTE) and All-cause Mortality During the Follow-up Period | Total Venous Thromboembolic Event (VTE) includes both proximal and distal deep vein thrombosis (DVT) (detected by routine bilateral venography), symptomatic DVT (confirmed by venous compression ultrasound, venography or autopsy) and pulmonary embolism (PE) (confirmed by pulmonary V-Q scintigraphy, chest x-ray, pulmonary angiography, spiral CT or autopsy). | 3 months |
| Number of Participants With Bleeding Events (Defined According to Modified McMaster Criteria) During Treatment Period | Major bleeding events were defined as
Clinically-relevant was defined as
Minor bleeding events were defined as all other bleeding events that did not fulfil the criteria from above. | First administration until 6-10 days |
| Blood Transfusion | Blood transfusion for treated and operated patients on Day of surgery. | Day 1 |
| Volume of Blood Loss | Volume of blood loss for treated and operated patients during surgery. | Day 1 |
| Laboratory Analyses | Frequency of patients with possible clinically significant abnormalities. | First administration to end of study |
| 1160.25.06106 Boehringer Ingelheim Investigational Site |
| Kogarah |
| New South Wales |
| Australia |
| 1160.25.06110 Boehringer Ingelheim Investigational Site | Lismore | New South Wales | Australia |
| 1160.25.06105 Boehringer Ingelheim Investigational Site | Bedford Park | South Australia | Australia |
| 1160.25.06107 Boehringer Ingelheim Investigational Site | Toorak Gardens | South Australia | Australia |
| 1160.25.06109 Boehringer Ingelheim Investigational Site | Woodville | South Australia | Australia |
| 1160.25.06104 Boehringer Ingelheim Investigational Site | Box Hill | Victoria | Australia |
| 1160.25.06102 Boehringer Ingelheim Investigational Site | Clayton | Victoria | Australia |
| 1160.25.06101 Boehringer Ingelheim Investigational Site | Malvern | Victoria | Australia |
| 1160.25.06103 Boehringer Ingelheim Investigational Site | Ringwood East | Victoria | Australia |
| 1160.25.06113 Boehringer Ingelheim Investigational Site | Windsor | Victoria | Australia |
| 1160.25.06111 Boehringer Ingelheim Investigational Site | Perth | Western Australia | Australia |
| 1160.25.04304 Boehringer Ingelheim Investigational Site | Linz | Austria |
| 1160.25.04302 Boehringer Ingelheim Investigational Site | Vienna | Austria |
| 1160.25.04303 Boehringer Ingelheim Investigational Site | Wels | Austria |
| 1160.25.04301 Boehringer Ingelheim Investigational Site | Wiener Neustadt | Austria |
| 1160.25.03207 UVC Brugmann | Brussels | Belgium |
| 1160.25.03209 ZOL St. Jan | Genk | Belgium |
| 1160.25.03206 Campus Sint-Lucas | Ghent | Belgium |
| 1160.25.03208 UZ Gent | Ghent | Belgium |
| 1160.25.03202 Virga Jesseziekenhuis | Hasselt | Belgium |
| 1160.25.03203 AZ Sint Elisabeth | Herentals | Belgium |
| 1160.25.03205 Ziekenhuis Oost-Limburg | Lanaken | Belgium |
| 1160.25.03201 UZ Gasthuisberg | Leuven | Belgium |
| 1160.25.42004 Boehringer Ingelheim Investigational Site | Brno-Bohunice | Czechia |
| 1160.25.42010 Boehringer Ingelheim Investigational Site | Chomutov | Czechia |
| 1160.25.42009 Boehringer Ingelheim Investigational Site | Havlíčkův Brod | Czechia |
| 1160.25.42002 Boehringer Ingelheim Investigational Site | Kladno | Czechia |
| 1160.25.42006 Boehringer Ingelheim Investigational Site | Kolín | Czechia |
| 1160.25.42003 Boehringer Ingelheim Investigational Site | Ostrava | Czechia |
| 1160.25.42001 Boehringer Ingelheim Investigational Site | Pilsen | Czechia |
| 1160.25.42007 Boehringer Ingelheim Investigational Site | Pradubice | Czechia |
| 1160.25.42005 Boehringer Ingelheim Investigational Site | Prague | Czechia |
| 1160.25.04571 Boehringer Ingelheim Investigational Site | Hellerup | Denmark |
| 1160.25.04570 Boehringer Ingelheim Investigational Site | Hørsholm | Denmark |
| 1160.25.04573 Boehringer Ingelheim Investigational Site | København NV | Denmark |
| 1160.25.04574 Boehringer Ingelheim Investigational Site | København S | Denmark |
| 1160.25.04575 Boehringer Ingelheim Investigational Site | Silkeborg | Denmark |
| 1160.25.35803 Boehringer Ingelheim Investigational Site | Helsinki | Finland |
| 1160.25.35802 Boehringer Ingelheim Investigational Site | Jyväskylä | Finland |
| 1160.25.35801 Boehringer Ingelheim Investigational Site | Oulu | Finland |
| 1160.25.35804 Boehringer Ingelheim Investigational Site | Seinäjoki | Finland |
| 1160.25.03304 Boehringer Ingelheim Investigational Site | Amiens | France |
| 1160.25.03307 Boehringer Ingelheim Investigational Site | Annecy | France |
| 1160.25.03305 Boehringer Ingelheim Investigational Site | La Rochelle | France |
| 1160.25.03301 Boehringer Ingelheim Investigational Site | Paris | France |
| 1160.25.03306 Boehringer Ingelheim Investigational Site | Poitiers | France |
| 1160.25.03303 Boehringer Ingelheim Investigational Site | Roubaix | France |
| 1160.25.03309 Boehringer Ingelheim Investigational Site | Saint-Etienne | France |
| 1160.25.03302 Boehringer Ingelheim Investigational Site | Soyaux | France |
| 1160.25.03308 Boehringer Ingelheim Investigational Site | Strasbourg | France |
| 1160.25.04906 Caritaskrankenhaus | Bad Mergentheim | Germany |
| 1160.25.04910 F.-A.-Universität Erlangen-Nürnberg | Erlangen | Germany |
| 1160.25.04904 Orthopädische Universitätsklinik | Frankfurt | Germany |
| 1160.25.04902 Klinikum Garmisch-Partenkirchen | Garmisch-Partenkirchen | Germany |
| 1160.25.04911 Martin-Luther-Universität Halle-Wittenberg | Halle | Germany |
| 1160.25.04912 Orthopädische Klinik Markgröningen gGmbH | Markgröningen | Germany |
| 1160.25.04901 Kreiskrankenhaus | Rheinfelden | Germany |
| 1160.25.04903 Hellmuth-Ulrici-Kliniken | Sommerfeld | Germany |
| 1160.25.04905 Aukammklinik | Wiesbaden | Germany |
| 1160.25.03607 Boehringer Ingelheim Investigational Site | Békéscsaba | Hungary |
| 1160.25.03603 Boehringer Ingelheim Investigational Site | Budapest | Hungary |
| 1160.25.03601 Boehringer Ingelheim Investigational Site | Gyula | Hungary |
| 1160.25.03604 Boehringer Ingelheim Investigational Site | Kecskemét | Hungary |
| 1160.25.03602 Boehringer Ingelheim Investigational Site | Szeged | Hungary |
| 1160.25.03605 Boehringer Ingelheim Investigational Site | Székesfehérvár | Hungary |
| 1160.25.03906 Boehringer Ingelheim Investigational Site | Bologna | Italy |
| 1160.25.03905 Boehringer Ingelheim Investigational Site | Parma | Italy |
| 1160.25.03901 Boehringer Ingelheim Investigational Site | Pavia | Italy |
| 1160.25.03903 Boehringer Ingelheim Investigational Site | Piacenza | Italy |
| 1160.25.03904 Boehringer Ingelheim Investigational Site | Reggio Emilia | Italy |
| 1160.25.03902 Boehringer Ingelheim Investigational Site | Treviso | Italy |
| 1160.25.03102 Boehringer Ingelheim Investigational Site | Amsterdam | Netherlands |
| 1160.25.03103 Boehringer Ingelheim Investigational Site | Hilversum | Netherlands |
| 1160.25.03101 Boehringer Ingelheim Investigational Site | Hoofddorp | Netherlands |
| 1160.25.03104 Boehringer Ingelheim Investigational Site | Nijmegen | Netherlands |
| 1160.25.03105 Boehringer Ingelheim Investigational Site | Sittard | Netherlands |
| 1160.25.03106 Boehringer Ingelheim Investigational Site | Zwolle | Netherlands |
| 1160.25.04804 Boehringer Ingelheim Investigational Site | Kielce | Poland |
| 1160.25.04806 Boehringer Ingelheim Investigational Site | Krakow | Poland |
| 1160.25.04807 Boehringer Ingelheim Investigational Site | Krakow | Poland |
| 1160.25.04803 Boehringer Ingelheim Investigational Site | Warsaw | Poland |
| 1160.25.02701 Boehringer Ingelheim Investigational Site | Bryanston | South Africa |
| 1160.25.02703 Boehringer Ingelheim Investigational Site | Randburg | South Africa |
| 1160.25.02702 Boehringer Ingelheim Investigational Site | Sandton | South Africa |
| 1160.25.03405 Boehringer Ingelheim Investigational Site | Alcorcón (Madrid) | Spain |
| 1160.25.03403 Boehringer Ingelheim Investigational Site | Barcelona | Spain |
| 1160.25.03411 Boehringer Ingelheim Investigational Site | Barcelona | Spain |
| 1160.25.03407 Boehringer Ingelheim Investigational Site | Hospitalet (Barcelona) | Spain |
| 1160.25.03409 Boehringer Ingelheim Investigational Site | Jaén | Spain |
| 1160.25.03401 Boehringer Ingelheim Investigational Site | Madrid | Spain |
| 1160.25.03402 Boehringer Ingelheim Investigational Site | Madrid | Spain |
| 1160.25.03404 Boehringer Ingelheim Investigational Site | Madrid | Spain |
| 1160.25.03406 Boehringer Ingelheim Investigational Site | Madrid | Spain |
| 1160.25.03408 Boehringer Ingelheim Investigational Site | Móstoles (Madrid) | Spain |
| 1160.25.03410 Boehringer Ingelheim Investigational Site | Valencia | Spain |
| 1160.25.04602 Boehringer Ingelheim Investigational Site | Falköping | Sweden |
| 1160.25.04601 Boehringer Ingelheim Investigational Site | Gothenburg | Sweden |
| 1160.25.04607 Boehringer Ingelheim Investigational Site | Halmstad | Sweden |
| 1160.25.04603 Boehringer Ingelheim Investigational Site | Kungälv | Sweden |
| 1160.25.04608 Boehringer Ingelheim Investigational Site | Lidköping | Sweden |
| 1160.25.04605 Boehringer Ingelheim Investigational Site | Linköping | Sweden |
| 1160.25.04604 Boehringer Ingelheim Investigational Site | Mölndal | Sweden |
| 1160.25.04610 Boehringer Ingelheim Investigational Site | Stockholm | Sweden |
| 1160.25.04609 Boehringer Ingelheim Investigational Site | Varberg | Sweden |
| FG002 |
| Enoxaparin |
40mg qd (once daily) subcutaneous |
| COMPLETED |
|
| NOT COMPLETED |
|
|
| Treatment |
|
|
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Dabigatran 220mg | qd (once daily) oral |
| BG001 | Dabigatran 150mg | qd (once daily) oral |
| BG002 | Enoxaparin | 40mg qd (once daily) subcutaneous |
| BG003 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | Years |
| |||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||
| Body Mass Index N=(677;702;692;2071) | Mean | Standard Deviation | kg/m^2 |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Participants With Total Venous Thromboembolic Event and All-cause Mortality During Treatment Period | Total Venous Thromboembolic Event (VTE) includes both proximal and distal deep vein thrombosis (DVT) (detected by routine bilateral venography), symptomatic DVT (confirmed by venous compression ultrasound, venography or autopsy) and pulmonary embolism (PE) (confirmed by pulmonary V-Q scintigraphy, chest x-ray, pulmonary angiography, spiral CT or autopsy). All of these components and all deaths were centrally adjudicated by the VTE events committee, which was not aware of the treatment allocation of the patients. | Full Analysis Set (all patients who had surgery and were randomised, received treatment, had an evaluable venogram for distal and proximal Deep Vein Thrombosis, or had confirmed symptomatic Deep Vein Thrombosis, Pulmonary Embolism, or had died) | Posted | Number | Participants | First administration until 6-10 days |
|
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With Major Venous Thromboembolic Event and Venous Thromboembolic Event-related Mortality During Treatment Period | Major Venous Thromboembolic Event (VTE) is defined as proximal DVT and PE, as adjudicated by the VTE events committee | Full Analysis Set - major (all patients who had surgery and were randomised, received treatment, had an evaluable venogram for proximal Deep Vein Thrombosis, or had confirmed symptomatic Deep Vein Thrombosis, Pulmonary Embolism, or had died by a Venous Thromboembolic Event-related death) | Posted | Number | Participants | First administration until 6-10 days |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With Proximal Deep Vein Thrombosis During Treatment Period | Proximal Deep Vein Thrombosis as adjudicated by the VTE events committee | Full Analysis Set - pDVT (all patients who had surgery and were randomised, received treatment, had an evaluable venogram for proximal Deep Vein Thrombosis, or had confirmed symptomatic Deep Vein Thrombosis) | Posted | Number | Participants | First administration until 6-10 days |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With Total Deep Vein Thrombosis During Treatment Period | Total Deep Vein Thrombosis as adjudicated by the VTE events committee | Full Analysis Set - tDVT (all patients who had surgery and were randomised, received treatment, had an evaluable venogram, or had confirmed symptomatic Deep Vein Thrombosis) | Posted | Number | Participants | First administration until 6-10 days |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With Symptomatic Deep Vein Thrombosis During Treatment Period | Symptomatic Deep Vein Thrombosis, confirmed by venous compression ultrasound, venography or autopsy, and as adjudicated by the VTE events committee | Full Analysis Set - op (all patients who are treated and operated) | Posted | Number | Participants | First administration until 6-10 days |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With Pulmonary Embolism During Treatment Period | Pulmonary embolism confirmed by pulmonary V-Q scintigraphy, chest x-ray, pulmonary angiography, spiral CT or autopsy, and as adjudicated by the VTE events committee | Full Analysis Set - op | Posted | Number | Participants | First administration until 6-10 days |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants Who Died During Treatment Period | All cause death, as adjudicated by the VTE events committee | Full Analysis Set - op | Posted | Number | Participants | First administration until 6-10 days |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With Total Venous Thromboembolic Event (VTE) and All-cause Mortality During the Follow-up Period | Total Venous Thromboembolic Event (VTE) includes both proximal and distal deep vein thrombosis (DVT) (detected by routine bilateral venography), symptomatic DVT (confirmed by venous compression ultrasound, venography or autopsy) and pulmonary embolism (PE) (confirmed by pulmonary V-Q scintigraphy, chest x-ray, pulmonary angiography, spiral CT or autopsy). | Patients with any data available during follow-up | Posted | Number | Participants | 3 months |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With Bleeding Events (Defined According to Modified McMaster Criteria) During Treatment Period | Major bleeding events were defined as
Clinically-relevant was defined as
Minor bleeding events were defined as all other bleeding events that did not fulfil the criteria from above. | Treated set | Posted | Number | Participants | First administration until 6-10 days |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Blood Transfusion | Blood transfusion for treated and operated patients on Day of surgery. | Posted | Number | participants | Day 1 |
|
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Volume of Blood Loss | Volume of blood loss for treated and operated patients during surgery. | Posted | Mean | Standard Deviation | mL | Day 1 |
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Laboratory Analyses | Frequency of patients with possible clinically significant abnormalities. | Treated patients | Posted | Number | participants | First administration to end of study |
|
|
First administration to end of study
Treatment emergent events (last medication + 3 days)
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Dabigatran 220mg | qd (once daily) oral | 31 | 679 | 405 | 679 | ||
| EG001 | Dabigatran 150mg | qd (once daily) oral | 44 | 703 | 438 | 703 | ||
| EG002 | Enoxaparin | 40mg qd (once daily) subcutaneous | 43 | 694 | 426 | 694 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Anaemia | Blood and lymphatic system disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Acute coronary syndrome | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Angina pectoris | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Atrial fibrillation | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Atrioventricular block | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Cardiac arrest | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Cardiac failure | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Coronary artery disease | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Intracardiac thrombus | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Left ventricular failure | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Myocardial infarction | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Myocardial ischaemia | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Tachycardia paroxysmal | Cardiac disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Abdominal pain | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Faeces discoloured | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Gastric haemorrhage | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Gastrointestinal motility disorder | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Haemorrhoidal haemorrhage | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Melaena | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Oesophagitis | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Rectal haemorrhage | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Subileus | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Chest pain | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Drug ineffective | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Impaired healing | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Oedema peripheral | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Pyrexia | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Secretion discharge | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Hepatitis | Hepatobiliary disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Bronchitis | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Device related infection | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Erysipelas | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Gastroenteritis | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Lower respiratory tract infection | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Postoperative infection | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Postoperative wound infection | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Staphylococcal sepsis | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Wound infection staphylococcal | Infections and infestations | MedDRA (9.1) | Systematic Assessment |
| |
| Arterial injury | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Dislocation of joint prosthesis | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Drug administration error | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Drug toxicity | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Fall | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Joint dislocation | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Post procedural haematoma | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Post procedural haemorrhage | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Procedural pain | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Traumatic haematoma | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
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| Wound secretion | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
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| Body temperature increased | Investigations | MedDRA (9.1) | Systematic Assessment |
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| Haemoglobin decreased | Investigations | MedDRA (9.1) | Systematic Assessment |
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| Hyponatraemia | Metabolism and nutrition disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Arthritis | Musculoskeletal and connective tissue disorders | MedDRA (9.1) | Systematic Assessment |
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| Haemarthrosis | Musculoskeletal and connective tissue disorders | MedDRA (9.1) | Systematic Assessment |
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| Joint instability | Musculoskeletal and connective tissue disorders | MedDRA (9.1) | Systematic Assessment |
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| Joint range of motion decreased | Musculoskeletal and connective tissue disorders | MedDRA (9.1) | Systematic Assessment |
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| Joint swelling | Musculoskeletal and connective tissue disorders | MedDRA (9.1) | Systematic Assessment |
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| Osteoarthritis | Musculoskeletal and connective tissue disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Pain in extremity | Musculoskeletal and connective tissue disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Colon neoplasm | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA (9.1) | Systematic Assessment |
| |
| Peroneal nerve palsy | Nervous system disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Syncope | Nervous system disorders | MedDRA (9.1) | Systematic Assessment |
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| Transient ischaemic attack | Nervous system disorders | MedDRA (9.1) | Systematic Assessment |
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| Bladder obstruction | Renal and urinary disorders | MedDRA (9.1) | Systematic Assessment |
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| Micturition disorder | Renal and urinary disorders | MedDRA (9.1) | Systematic Assessment |
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| Prostatitis | Reproductive system and breast disorders | MedDRA (9.1) | Systematic Assessment |
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| Asthma | Respiratory, thoracic and mediastinal disorders | MedDRA (9.1) | Systematic Assessment |
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| Dyspnoea | Respiratory, thoracic and mediastinal disorders | MedDRA (9.1) | Systematic Assessment |
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| Pulmonary embolism | Respiratory, thoracic and mediastinal disorders | MedDRA (9.1) | Systematic Assessment |
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| Pulmonary oedema | Respiratory, thoracic and mediastinal disorders | MedDRA (9.1) | Systematic Assessment |
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| Respiratory depression | Respiratory, thoracic and mediastinal disorders | MedDRA (9.1) | Systematic Assessment |
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| Scar | Skin and subcutaneous tissue disorders | MedDRA (9.1) | Systematic Assessment |
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| Immobilisation prolonged | Social circumstances | MedDRA (9.1) | Systematic Assessment |
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| Deep vein thrombosis | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Haematoma | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Haemorrhage | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Hypertension | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Hypertensive crisis | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Shock | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Thrombophlebitis superficial | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Thrombosis | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Wound haemorrhage | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Constipation | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
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| Diarrhoea | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
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| Nausea | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Oedema peripheral | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Pyrexia | General disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Post procedural haematoma | Injury, poisoning and procedural complications | MedDRA (9.1) | Systematic Assessment |
| |
| Insomnia | Psychiatric disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Deep vein thrombosis | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
| |
| Hypotension | Vascular disorders | MedDRA (9.1) | Systematic Assessment |
|
Any publication of the result of this trial must be consistent with the Boehringer Ingelheim publication policy. The rights of the investigator and of the sponsor with regard to publication of the results of this trial are described in the investigator contract
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Boehringer Ingelheim Call Center | Boehringer Ingelheim Pharmaceuticals | 1-800-243-0127 | clintriage.rdg@boehringer-ingelheim.com |
| ID | Term |
|---|---|
| D013923 | Thromboembolism |
| ID | Term |
|---|---|
| D016769 | Embolism and Thrombosis |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D017984 | Enoxaparin |
| D000069604 | Dabigatran |
| ID | Term |
|---|---|
| D006495 | Heparin, Low-Molecular-Weight |
| D006493 | Heparin |
| D006025 | Glycosaminoglycans |
| D011134 | Polysaccharides |
| D002241 | Carbohydrates |
| D011725 | Pyridines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D001562 | Benzimidazoles |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
Not provided
Not provided
| Withdrawal by Subject |
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| Other |
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| Male |
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| Risk difference versus Enoxaparin | Normal approximation | Normal approximation of independent binomial distribution without stratification | 0.3553 | p-value is for superiority testing | Risk Difference (Percentage) | 2.8 | 95 | -3.1 | 8.7 | Yes | Non-Inferiority or Equivalence | Non-inferiority Analysis with NI margin 9.2%. This results from the null-hypotheses of non-inferiority testing, where the absolute risk difference has to be below 9.2%. Non-inferiority can only be shown with CI. |
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| Enoxaparin |
40mg qd (once daily) subcutaneous |
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