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| Name | Class |
|---|---|
| Canadian Institutes of Health Research (CIHR) | OTHER_GOV |
| National Health and Medical Research Council, Australia | OTHER |
| Baxter Healthcare Corporation | INDUSTRY |
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The objectives of this trial are to determine whether, in critically ill patients with severe acute kidney injury (AKI), randomization to accelerated initiation of renal replacement therapy (RRT), compared to standard initiation, leads to:
Acute kidney injury (AKI) is a common and devastating complication of critical illness. Once AKI is established, treatment is largely supportive and no intervention has been found to restore kidney function or improve overall survival. Renal replacement therapy (RRT), usually in the form of hemodialysis, is frequently needed to manage patients with severe AKI. Such patients have an in-hospital mortality that consistently exceeds 50% with delays in RRT initiation implicated as a possible contributor. A recent meta-analysis suggested that earlier initiation of RRT may improve survival, but this is based on data derived overwhelmingly from observational studies. The investigators recently completed a multi-centre randomized controlled pilot trial that confirmed the feasibility of allocating patients to two different strategies of RRT initiation. Patient recruitment and follow-up, as well as patient safety, were successfully demonstrated during the pilot phase of this research program. The optimal timing of RRT initiation is an existing knowledge gap and a clear priority for investigation.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Standard RRT initiation | Active Comparator | RRT initiation will be guided by the presence of one or more clinical indications. Even in the absence of one of these indications, RRT may be commenced at the discretion of the treating physician. |
|
| Accelerated RRT initiation | Experimental | A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of the patient meeting the eligibility criteria. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Standard RRT initiation | Other | In the absence of kidney function recovery, the initiation of RRT will be permitted if one of the following develops: serum potassium ≥ 6.0 mmol/L; pH ≤ 7.20 or serum bicarbonate ≤ 12 mmol/L; evidence of severe respiratory failure, based on a PaO2/FiO2 ≤ 200 and clinical perception of volume overload; and/or persistent AKI > 72 hours following the time of randomization. |
| Measure | Description | Time Frame |
|---|---|---|
| All-cause Mortality. | 90 days following study randomization. |
| Measure | Description | Time Frame |
|---|---|---|
| RRT Dependence | 90 days following study randomization. | |
| Composite of Death or RRT Dependence. | 90 days following study randomization. | |
| Measurement of Estimated Glomerular Filtration Rate. |
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Inclusion Criteria:
Age ≥ 18 years
Admission to an intensive care unit (ICU)
Evidence of kidney dysfunction [serum creatinine ≥100 µmol/L (women) and ≥ 130 µmol/L (men)]
Evidence of severe AKI defined by at least 1 of the following 3 criteria:
i) ≥ 2-fold increase in serum creatinine from a known pre-morbid baseline or during the current hospitalization; OR ii) Achievement of a serum creatinine ≥ 354 µmol/L with evidence of a minimum increase of 27 µmol/L from pre-morbid baseline or during the current hospitalization; OR iii) Urine output < 6.0 mL/kg over the preceding 12 hours
Exclusion Criteria:
Serum potassium > 5.5 mmol/L
Serum bicarbonate < 15 mmol/L
Presence of a drug overdose that necessitates initiation of RRT
Lack of commitment to ongoing life support (including RRT)
Any RRT within the previous 2 months (either acute or chronic RRT)
Kidney transplant within the past 365 days
Known pre-hospitalization advanced chronic kidney disease, defined by an estimated glomerular filtration rate < 20 mL/min/1.73 m2
Presence or clinical suspicion of renal obstruction, rapidly progressive glomerulonephritis, vasculitis, thrombotic microangiopathy or acute interstitial nephritis
Clinician(s) caring for patient believe(s) that immediate RRT is mandated
Clinician(s) caring for patient believe(s) that deferral of RRT initiation is mandated
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| Name | Affiliation | Role |
|---|---|---|
| Ron Wald, MDCM MPH | Unity Health Toronto | Principal Investigator |
| Sean M Bagshaw, MD MSc | University of Alberta | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Alabama at Birmingham | Birmingham | Alabama | 35294 | United States | ||
| University of Florida |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 40232884 | Derived | McCoy IE, Liu KD, Ghamarian E, Quenot JP, Zarbock A, Bihorac A, Khoo B, Gallagher MP, Du B, Joannidis M, Kashani K, Tolwani A, Bagshaw SM, Wald R; STandard versus Accelerated initiation of Renal Replacement Therapy in AKI (STARRT-AKI) Investigators. Dialysis Dependence in Standard versus Accelerated Initiation of KRT in AKI: A Post Hoc Analysis. Clin J Am Soc Nephrol. 2025 May 1;20(5):601-607. doi: 10.2215/CJN.0000000672. Epub 2025 Mar 11. | |
| 38461657 |
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| ID | Title | Description |
|---|---|---|
| FG000 | Standard RRT Initiation | RRT initiation will be guided by the presence of one or more clinical indications. Even in the absence of one of these indications, RRT may be commenced at the discretion of the treating physician. Standard RRT initiation: In the absence of kidney function recovery, the initiation of RRT will be permitted if one of the following develops: serum potassium ≥ 6.0 mmol/L; pH ≤ 7.20 or serum bicarbonate ≤ 12 mmol/L; evidence of severe respiratory failure, based on a PaO2/FiO2 ≤ 200 and clinical perception of volume overload; and/or persistent AKI > 72 hours following the time of randomization. |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Oct 5, 2015 | Jan 3, 2023 |
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| The George Institute |
| OTHER |
| National Institute for Health Research, United Kingdom | OTHER_GOV |
| Medical Research Institute of New Zealand | OTHER |
| Health Research Council, New Zealand | OTHER |
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|
| Accelerated RRT initiation | Other | A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of eligibility. This 12 hour window includes the time needed to obtain consent. |
|
| 90 days following study randomization. |
| Measurement of Albuminuria. | 90 days following study randomization. |
| Major Adverse Kidney Outcomes. | Defined as death, RRT dependence or sustained reduction in kidney function (defined as eGFR < 75% baseline eGFR). | 90 days following study randomization. |
| Mechanical Ventilation-free Days. | Measured from randomization through day 28. |
| Vasoactive Therapy-free Days | Measured from randomization through day 28. |
| ICU-free Days | Measured from randomization through day 28. |
| Hospitalization-free Days | Measured from randomization through day 90. |
| Death in ICU | Measured in-hospital and at day 28. |
| EuroQoL EQ-5D-5L. | A measure of health-related quality of life and patient utility. | Measured at day 90 and at day 365. |
| Health Care Costs. | Measured from baseline through day 365. |
| Composite of Death or RRT Dependence. | Measured at day 365. |
| Gainesville |
| Florida |
| 32611 |
| United States |
| University of Kentucy | Lexington | Kentucky | 40506 | United States |
| Mayo Clinic | Rochester | Minnesota | 55905 | United States |
| Rhode Island Hospital | Providence | Rhode Island | 02903 | United States |
| The Miriam Hospital | Providence | Rhode Island | 02906 | United States |
| Ballarat Hospital | Ballarat | 3350 | Australia |
| Flinder Medical Centre | Bedford Park | 5042 | Australia |
| Bendigo Hospital | Bendigo | 3550 | Australia |
| Eastern Hospital (Box Hill and Maroondah Hospital) | Box Hill | Australia |
| Concord Hospital | Concord | 2139 | Australia |
| The Northern Hospital | Epping | 3076 | Australia |
| Geelong Hospital | Geelong | 3220 | Australia |
| Austin Hospital | Heidelberg | 3084 | Australia |
| Nepean Hospital | Kingswood | NSW 2747 | Australia |
| The Alfred Hospital | Melbourne | Australia |
| Nambour General Hospital | Nambour | QLD 4560 | Australia |
| Western Health (Footscray Hospital & Sunshine Hospital) | St Albans | VIC 3021 | Australia |
| St. Vincent's Hospital | Sydney | 2010 | Australia |
| Royal North Shore Hospital | Sydney | 2065 | Australia |
| Royal Prince Alfred Hospital | Sydney | Australia |
| Princess Alexandra Hospital | Woolloongabba | Australia |
| Medical University Graz | Graz | 8036 | Austria |
| Medical University Innsbruck | Innsbruck | Austria |
| Vienna General Hospital | Vienna | 1090 | Austria |
| Antwerp University Hospital | Edegem | 2650 | Belgium |
| Ghent University Hospital | Ghent | Belgium |
| Hospital de Clínicas de Porto Alegre - Rio Grande do Sul | Rio Branco | Brazil |
| Peter Lougheed Centre | Calgary | Alberta | T1Y 6J4 | Canada |
| Foothills Hospital | Calgary | Alberta | Canada |
| Misericordia Community Hospital | Edmonton | Alberta | T5R 4H5 | Canada |
| Mazankowski Alberta Heart Institute | Edmonton | Alberta | T6G 2B7 | Canada |
| University of Alberta Hospital | Edmonton | Alberta | T6G 2B7 | Canada |
| Grey Nuns Community Hospital | Edmonton | Alberta | Canada |
| Royal Alexandra Hospital | Edmonton | Alberta | Canada |
| Red Deer Regional Hospital | Red Deer | Alberta | T4N 4E7 | Canada |
| Sturgeon Community Hospital | St. Albert | Alberta | T8N 6C4 | Canada |
| Surrey Memorial Hospital, Fraser Health | Surrey | British Columbia | V3V 1Z2 | Canada |
| St. Paul's Hospital - Providence Health Care | Vancouver | British Columbia | Canada |
| Royal Jubilee Hospital | Victoria | British Columbia | V8R 1J8 | Canada |
| Victoria General Hospital | Victoria | British Columbia | V8Z 6R5 | Canada |
| Health Sciences Centre | Winnipeg | Manitoba | Canada |
| Memorial University of Newfoundland | St. John's | Newfoundland and Labrador | A1B 3X9 | Canada |
| Health Sciences North | Greater Sudbury | Ontario | Canada |
| Hamilton General Hospital | Hamilton | Ontario | Canada |
| Juravinski Hospital | Hamilton | Ontario | Canada |
| St. Joseph's Healthcare Hamilton | Hamilton | Ontario | Canada |
| Kingston General Hospital | Kingston | Ontario | Canada |
| London Health Sciences Centre, University Hospital | London | Ontario | Canada |
| London Health Sciences Centre, Victoria Hospital | London | Ontario | Canada |
| Trillium Health Partners - Credit Valley Hospital | Mississauga | Ontario | Canada |
| Trillium Health Partners - Mississauga Hospital | Mississauga | Ontario | Canada |
| Lakeridge Health | Oshawa | Ontario | L1G 2B9 | Canada |
| The Ottawa Hospital, Civic Campus | Ottawa | Ontario | Canada |
| The Ottawa Hospital, General Campus | Ottawa | Ontario | Canada |
| Mount Sinai Hospital | Toronto | Ontario | Canada |
| St. Michael's Hospital | Toronto | Ontario | Canada |
| Sunnybrook Health Sciences Centre | Toronto | Ontario | Canada |
| Toronto General Hospital | Toronto | Ontario | Canada |
| Toronto Western Hospital | Toronto | Ontario | Canada |
| Centre hospitalier de l'université de Montréal (Notre Dame) | Montreal | Quebec | Canada |
| Centre hospitalier de l'université de Montréal (St. Luc) | Montreal | Quebec | Canada |
| CHUM - Hôtel Dieu Montreal | Montreal | Quebec | Canada |
| Hopital Maisonneuve-Rosemont | Montreal | Quebec | Canada |
| McGill University Health Centre (MUHC) | Montreal | Quebec | Canada |
| Institut Universitaire de Cardiologie et de Pneumologie de Québec- Université Laval (IUCPQ) | Québec | Quebec | G1V 4G5 | Canada |
| Centre Hospitalier Universitaire de Quebec (CHUQ) | Québec | Quebec | Canada |
| Centre Hôspitalier universitaire de Sherbrooke (CHUS) | Sherbrooke | Quebec | Canada |
| Centre de sante et de services sociaux de Trois-Rivieres (CIUSSS MCQ) | Trois-Rivières | Quebec | Canada |
| Regina Qu'Appelle Health Region | Saskatoon | Saskatchewan | Canada |
| Beijing Friendship Hospital, Capital Medical University | Beijing | China |
| Peking Union Medical College Hospital | Beijing | China |
| The First Hospital of Jilin University | Changchun | China |
| Xiangya Hospital Central South University | Changsha | China |
| Guizhou Provincial People's Hospital | Guiyang | China |
| Shandong Provincial Hospital | Jinan | China |
| Zhongda Hospital Southeast University | Nanjing | China |
| Renmin Hospital of Wuhan University | Wuhan | China |
| Zhongnan Hospital of Wuhan University | Wuhan | China |
| The First Affiliated Hospital of Xi'An Jiaotong University | Xi'an | China |
| The First Affiliated Hospital of Xiamen University | Xiamen | China |
| Henan Provincial People's Hospital | Zhengzhou | China |
| Helsinki University Central Hospital | Helsinki | 00290 | Finland |
| Tampere University Hospital | Tampere | 33521 | Finland |
| Turku University Hospital | Turku | 20521 | Finland |
| Hopital Louis Mourier | Colombes | 92700 | France |
| Klinikum Coburg | Coburg | 96450 | Germany |
| University Hospital Münster | Münster | 48149 | Germany |
| St. Vincent's University Hospital | Dublin | Ireland |
| San Raffaele Hospital | Milan | 20132 | Italy |
| Auckland City Hospital | Grafton | Auckland | 1148 | New Zealand |
| Auckland Hospital DCCM | Auckland | New Zealand |
| Christchurch Hospital | Christchurch | 8011 | New Zealand |
| Hawke's Bay Hospital | Hastings | New Zealand |
| Rotorua Hospital | Rotorua | New Zealand |
| Wellington Hospital | Wellington | 6021 | New Zealand |
| Centre Hospitalier Universitaire Vaudois (CHUV) | Lausanne | 1011 | Switzerland |
| Stoke Mandeville Hospital | Aylesbury | HP21 8AL | United Kingdom |
| Wycombe General Hospital | High Wycombe | HP11 2TT | United Kingdom |
| Leeds Teaching Hospital | Leeds | United Kingdom |
| Lewisham Hospital | London | SE13 6LH | United Kingdom |
| King's College Hospital | London | SE5 9RS | United Kingdom |
| Guy's and St. Thomas Hospital | London | United Kingdom |
| Nottingham University Hospital | Nottingham | NG5 1PB | United Kingdom |
| Princess Royal University Hospital | Orpington | BR6 8ND | United Kingdom |
| Derived |
| Zampieri FG, Serpa-Neto A, Wald R, Bellomo R, Bagshaw SM; STARRT-AKI and RENAL Investigators. Hierarchical endpoints in critical care: A post-hoc exploratory analysis of the standard versus accelerated initiation of renal-replacement therapy in acute kidney injury and the intensity of continuous renal-replacement therapy in critically ill patients trials. J Crit Care. 2024 Aug;82:154767. doi: 10.1016/j.jcrc.2024.154767. Epub 2024 Mar 11. |
| 38380940 | Derived | Vaara ST, Serpa Neto A, Bellomo R, Adhikari NKJ, Dreyfuss D, Gallagher M, Gaudry S, Hoste E, Joannidis M, Pettila V, Wang AY, Kashani K, Wald R, Bagshaw SM, Ostermann M; STandard vs. Accelerated initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) Investigators. Regional Practice Variation and Outcomes in the Standard Versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) Trial: A Post Hoc Secondary Analysis. Crit Care Explor. 2024 Feb 19;6(2):e1053. doi: 10.1097/CCE.0000000000001053. eCollection 2024 Feb. |
| 36424662 | Derived | Wald R, Kirkham B, daCosta BR, Ghamarian E, Adhikari NKJ, Beaubien-Souligny W, Bellomo R, Gallagher MP, Goldstein S, Hoste EAJ, Liu KD, Neyra JA, Ostermann M, Palevsky PM, Schneider A, Vaara ST, Bagshaw SM. Fluid balance and renal replacement therapy initiation strategy: a secondary analysis of the STARRT-AKI trial. Crit Care. 2022 Nov 24;26(1):360. doi: 10.1186/s13054-022-04229-0. |
| 36416787 | Derived | Fayad AI, Buamscha DG, Ciapponi A. Timing of kidney replacement therapy initiation for acute kidney injury. Cochrane Database Syst Rev. 2022 Nov 23;11(11):CD010612. doi: 10.1002/14651858.CD010612.pub3. |
| 32668114 | Derived | STARRT-AKI Investigators; Canadian Critical Care Trials Group; Australian and New Zealand Intensive Care Society Clinical Trials Group; United Kingdom Critical Care Research Group; Canadian Nephrology Trials Network; Irish Critical Care Trials Group; Bagshaw SM, Wald R, Adhikari NKJ, Bellomo R, da Costa BR, Dreyfuss D, Du B, Gallagher MP, Gaudry S, Hoste EA, Lamontagne F, Joannidis M, Landoni G, Liu KD, McAuley DF, McGuinness SP, Neyra JA, Nichol AD, Ostermann M, Palevsky PM, Pettila V, Quenot JP, Qiu H, Rochwerg B, Schneider AG, Smith OM, Thome F, Thorpe KE, Vaara S, Weir M, Wang AY, Young P, Zarbock A. Timing of Initiation of Renal-Replacement Therapy in Acute Kidney Injury. N Engl J Med. 2020 Jul 16;383(3):240-251. doi: 10.1056/NEJMoa2000741. |
| 31462203 | Derived | STARRT-AKI Investigators. Statistical analysis plan for the Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial. Crit Care Resusc. 2019 Sep;21(3):162-170. |
| 31218013 | Derived | STARRT-AKI Investigators. STandard versus Accelerated initiation of Renal Replacement Therapy in Acute Kidney Injury: Study Protocol for a Multi-National, Multi-Center, Randomized Controlled Trial. Can J Kidney Health Dis. 2019 Jun 10;6:2054358119852937. doi: 10.1177/2054358119852937. eCollection 2019. |
| FG001 | Accelerated RRT Initiation | A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of the patient meeting the eligibility criteria. Accelerated RRT initiation: A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of eligibility. This 12 hour window includes the time needed to obtain consent. |
| Withdrew Consent |
|
| Randomized Non-eligible |
|
| Lost to Follow-up |
|
| COMPLETED |
|
| NOT COMPLETED |
|
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Standard RRT Initiation | RRT initiation will be guided by the presence of one or more clinical indications. Even in the absence of one of these indications, RRT may be commenced at the discretion of the treating physician. Standard RRT initiation: In the absence of kidney function recovery, the initiation of RRT will be permitted if one of the following develops: serum potassium ≥ 6.0 mmol/L; pH ≤ 7.20 or serum bicarbonate ≤ 12 mmol/L; evidence of severe respiratory failure, based on a PaO2/FiO2 ≤ 200 and clinical perception of volume overload; and/or persistent AKI > 72 hours following the time of randomization. |
| BG001 | Accelerated RRT Initiation | A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of the patient meeting the eligibility criteria. Accelerated RRT initiation: A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of eligibility. This 12 hour window includes the time needed to obtain consent. |
| BG002 | 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 |
| ||||||||||||||||
| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
| |||||||||||||||
| Region of Enrollment | Number | participants |
| ||||||||||||||||
| Weight - kg | Number analyzed differs from number enrolled due to missing data. | Mean | Standard Deviation | kg |
| ||||||||||||||
| Serum creatinine - mg/dl | Mean | Standard Deviation | mg/dl |
| |||||||||||||||
| Estimated glomerular filtration rate - ml/min/1.73 m2 | Mean | Standard Deviation | ml/min/1.73 m2 |
| |||||||||||||||
| Preexisting conditions - no./total no. (%) - Chronic kidney disease | Count of Participants | Participants |
| ||||||||||||||||
| Preexisting conditions - no./total no. (%) - Hypertension | Count of Participants | Participants |
| ||||||||||||||||
| Preexisting conditions - no./total no. (%) - Diabetes mellitus | Data for this variable was missing for one participant in the standard arm. | Count of Participants | Participants |
| |||||||||||||||
| Preexisting conditions - no./total no. (%) - Heart failure | Data for this variable was missing for one participant in the standard arm. | Count of Participants | Participants |
| |||||||||||||||
| Preexisting conditions - no./total no. (%) - Coronary artery disease | Data for this variable was missing for one participant in the standard arm. | Count of Participants | Participants |
| |||||||||||||||
| Preexisting conditions - no./total no. (%) - Liver disease | Data for this variable was missing for one participant in the standard arm. | Count of Participants | Participants |
| |||||||||||||||
| Preexisting conditions - no./total no. (%) - Metastatic cancer | Count of Participants | Participants |
| ||||||||||||||||
| Preexisting conditions - no./total no. (%) - Hematologic cancer | Count of Participants | Participants |
| ||||||||||||||||
| Preexisting conditions - no./total no. (%) - HIV infection or AIDS | Count of Participants | Participants |
| ||||||||||||||||
| Admission category - no. (%) - Scheduled surgery | Count of Participants | Participants |
| ||||||||||||||||
| Admission category - no. (%) - Unscheduled surgery | Count of Participants | Participants |
| ||||||||||||||||
| Admission category - no. (%) - Medical | Count of Participants | Participants |
| ||||||||||||||||
| Hospital-acquired risk factor for AKI in previous wk - no./total no. (%) - Cardiopulmonary bypass | Count of Participants | Participants |
| ||||||||||||||||
| Hospital-acquired risk factor for AKI in previous wk - no./total no. (%) - Aortic aneurysm repair | Missing data | Count of Participants | Participants |
| |||||||||||||||
| Hospital-acquired risk factor for AKI in previous wk - no./total no. (%) - Other vascular surgery | Count of Participants | Participants |
| ||||||||||||||||
| Hospital-acquired risk factor for AKI in previous wk - no./total no. (%) - Major trauma | Count of Participants | Participants |
| ||||||||||||||||
| Hospital-acquired risk factor for AKI in previous wk - no./total no. (%) - Obstetric complication | Count of Participants | Participants |
| ||||||||||||||||
| Hospital-acquired risk factor AKI previous wk (no./total no. (%)) - Exposure radiocontrast material | Missing data | Count of Participants | Participants |
| |||||||||||||||
| Hospital-acquired risk factor for AKI in previous wk - no./total no. (%) - Receipt of aminoglycoside | Missing data | Count of Participants | Participants |
| |||||||||||||||
| Hospital-acquired risk factor for AKI in previous wk - no./total no. (%) - Receipt of amphotericin B | Missing data | Count of Participants | Participants |
| |||||||||||||||
| Clinical condition at randomization - Sepsis - no. (%) | Count of Participants | Participants |
| ||||||||||||||||
| Clinical condition at randomization - Septic shock - no. (%) | Count of Participants | Participants |
| ||||||||||||||||
| Clinical condition at randomization - SAPS II value | Results for the Simplified Acute Physiology Score (SAPS) II range from 0 to 163, with higher scores indicating more severe disease and a higher risk of death. | Mean | Standard Deviation | units on a scale |
| ||||||||||||||
| Clinical condition at randomization - SOFA score | Scores on the Sequential Organ Failure Assessment (SOFA) range from 0 to 24, with higher scores indicating more severe disease and a higher risk of death | Mean | Standard Deviation | SOFA score (0-24) |
| ||||||||||||||
| Clinical condition at randomization - Mechanical ventilation - no. (%) | Count of Participants | Participants |
| ||||||||||||||||
| Clinical condition at randomization - Vasoactive support - no. (%) | Count of Participants | Participants |
| ||||||||||||||||
| Clinical condition at randomization - Serum creatinine - mg/dl | At baseline, the serum creatinine level was defined as the most recent outpatient level obtained during the year pre-ceding the current hospitalization. If this value was not available, the lowest serum creatinine level obtained during the current hospitalization was used to establish the baseline. This serum creatinine value was obtained at randomization. | Mean | Standard Deviation | mg/dl |
| ||||||||||||||
| Clinical condition at randomization - Serum potassium - mmol/liter | Mean | Standard Deviation | mmol/liter |
| |||||||||||||||
| Clinical condition at randomization - Serum bicarbonate - mmol/liter | Mean | Standard Deviation | mmol/liter |
| |||||||||||||||
| Clinical condition at randomization - Median urinary output (IQR) - ml/24 hr | Mean | Inter-Quartile Range | ml/24 hr |
| |||||||||||||||
| Clinical condition at randomization- Oliguria or anuria - no./total no. (%) | Missing data | Count of Participants | Participants |
| |||||||||||||||
| Clinical condition at randomization- Median cumulative fluid balance (IQR) - ml | Mean | Inter-Quartile Range | ml/ 24 hr |
|
| 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 | All-cause Mortality. | Posted | Count of Participants | Participants | No | 90 days following study randomization. |
|
|
| ||||||||||||||||||||||||||||||
| Secondary | RRT Dependence | Not Posted | 90 days following study randomization. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Composite of Death or RRT Dependence. | Not Posted | 90 days following study randomization. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Measurement of Estimated Glomerular Filtration Rate. | Not Posted | 90 days following study randomization. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Measurement of Albuminuria. | Not Posted | 90 days following study randomization. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Major Adverse Kidney Outcomes. | Defined as death, RRT dependence or sustained reduction in kidney function (defined as eGFR < 75% baseline eGFR). | Not Posted | 90 days following study randomization. | Participants | ||||||||||||||||||||||||||||||||||
| Secondary | Mechanical Ventilation-free Days. | Not Posted | Measured from randomization through day 28. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Vasoactive Therapy-free Days | Not Posted | Measured from randomization through day 28. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | ICU-free Days | Not Posted | Measured from randomization through day 28. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Hospitalization-free Days | Not Posted | Measured from randomization through day 90. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Death in ICU | Not Posted | Measured in-hospital and at day 28. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | EuroQoL EQ-5D-5L. | A measure of health-related quality of life and patient utility. | Not Posted | Measured at day 90 and at day 365. | Participants | ||||||||||||||||||||||||||||||||||
| Secondary | Health Care Costs. | Not Posted | Measured from baseline through day 365. | Participants | |||||||||||||||||||||||||||||||||||
| Secondary | Composite of Death or RRT Dependence. | Not Posted | Measured at day 365. | Participants |
Through study completion, 90 days following study randomization
All-Cause Mortality was pre-specified to be monitored/assessed only in participants who completed the study. AEs and SAEs were reported from the entire randomized population minus those who withdrew consent
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 | Standard RRT Initiation | RRT initiation will be guided by the presence of one or more clinical indications. Even in the absence of one of these indications, RRT may be commenced at the discretion of the treating physician. Standard RRT initiation: In the absence of kidney function recovery, the initiation of RRT will be permitted if one of the following develops: serum potassium ≥ 6.0 mmol/L; pH ≤ 7.20 or serum bicarbonate ≤ 12 mmol/L; evidence of severe respiratory failure, based on a PaO2/FiO2 ≤ 200 and clinical perception of volume overload; and/or persistent AKI > 72 hours following the time of randomization. | 639 | 1,462 | 8 | 1,489 | 245 | 1,489 |
| EG001 | Accelerated RRT Initiation | A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of the patient meeting the eligibility criteria. Accelerated RRT initiation: A dialysis catheter will be placed and RRT initiated as soon as possible and within 12 hours of eligibility. This 12 hour window includes the time needed to obtain consent. | 643 | 1,465 | 15 | 1,503 | 346 | 1,503 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Arrhythmia during RRT | Cardiac disorders | Systematic Assessment |
| ||
| CVC - associated bloodstream infection | Surgical and medical procedures | Systematic Assessment |
| ||
| Hemorrhage at site of CVC insertion | Surgical and medical procedures | Systematic Assessment |
| ||
| Hemothorax following CVC insertion | Surgical and medical procedures | Systematic Assessment |
| ||
| Major bleeding | Surgical and medical procedures | Systematic Assessment |
| ||
| Pneumothorax following CVC insertion | Surgical and medical procedures | Systematic Assessment |
| ||
| RRT - associated hypotension | Vascular disorders | Systematic Assessment |
| ||
| Severe hypocalcemia (Ionized calcium < 0.90 mmol/L) | General disorders | Systematic Assessment |
| ||
| Other | General disorders | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Hypotension | Vascular disorders | Systematic Assessment |
| ||
| Arrhythmia | Cardiac disorders | Systematic Assessment |
| ||
| Seizure | Nervous system disorders | Systematic Assessment |
| ||
| Bleeding | Surgical and medical procedures | Systematic Assessment |
| ||
| Allergic reaction | Surgical and medical procedures | Systematic Assessment |
| ||
| Decreased phosphate (<0.5 mmol/liter) | General disorders | Systematic Assessment |
| ||
| Decreased potassium (<3.0 mmol/liter) | General disorders | Systematic Assessment |
| ||
| Decreased ionized calcium (<0.90 mmol/ liter) | General disorders | Systematic Assessment |
| ||
| Pneumothorax or hemothorax | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
| ||
| Thrombus (as confirmed on ultrasonography) | Vascular disorders | Systematic Assessment |
| ||
| Arterial puncture | Surgical and medical procedures | Systematic Assessment |
| ||
| Bloodstream infection | Infections and infestations | Systematic Assessment |
| ||
| Other | General disorders | Systematic Assessment |
|
Not provided
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Ron Wald | Unity Health Toronto | (416) 867-3703 | ron.wald@unityhealth.to |
| Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | May 23, 2019 | Jul 26, 2024 | SAP_001.pdf |
| ICF | No | No | Yes | Informed Consent Form | Feb 2, 2016 | Jan 3, 2023 | ICF_002.pdf |
| ID | Term |
|---|---|
| D058186 | Acute Kidney Injury |
| D016638 | Critical Illness |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
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