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| ID | Type | Description | Link |
|---|---|---|---|
| 2011-005797-32 | EudraCT Number | ||
| DRKS00004353 | Other Identifier | DRKS |
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| Name | Class |
|---|---|
| Teva Branded Pharmaceutical Products R&D, Inc. | INDUSTRY |
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"Episodic breathlessness (or dyspnea) is one form of chronic refractory breathlessness characterized by a severe worsening of breathlessness intensity or unpleasantness beyond usual fluctuations in the patient's perception. Episodes are time-limited (seconds to hours) and occur intermittently, with or without underlying continuous breathlessness. Episodes may be predictable or unpredictable, depending on whether any trigger(s) can be identified. There is a range of known triggers which can interact (e.g. exertion, emotions, comorbidities or external environment). One episode can be caused by one or more triggers." ( definition by an international expert consensus [Simon et al. 2013]). Approximately half of patients with cancer complain about breathlessness with the highest prevalence in pulmonary malignancies. Episodic breathlessness is reported by 81% of breathless cancer patients with significant impairment on quality of life and limitations on activity. Although episodic breathlessness show some similar characteristics like episodes of pain (breakthrough cancer pain, BTCP; median duration 30minutes), they are often shorter: 91% last less than 20minutes (min). Other evidence supports these findings with duration between 2-15minutes which is a real challenge for the treatment of episodic breathlessness. In the majority of cases, episodic breathlessness occur 1-4 times per day and peak intensity is rated moderate or severe.
There is evidence for the effectiveness of opioids for the relief of chronic refractory breathlessness. There is no evaluated and proven standard treatment for the relief of episodic breathlessness at the moment but immediate-release morphine (IRM) as solution or tablet is most frequently used in clinical practice to treat episodic breathlessness. Time to onset of action of IRM is about 20-30min for pain. Fentanyl is a potent opioid and shows good evidence for the treatment of BTCP through its quick onset of action (5-15min) and short duration of action (50-60min). Because of its pharmacodynamic properties fentanyl might be appropriate and effective for the relief of episodic breathlessness. However, the efficacy of fentanyl for the relief of breathlessness and time to onset is unknown.
This pilot study aims to evaluate relative efficacy, feasibility and time to onset of two different opioids (fentanyl and morphine) in order to improve the management of episodic breathlessness.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Fentanyl | Experimental | Fentanyl buccal tablet Dosage: 100µg - 600 µg Fentanyl (to be determined by titration) Administration: buccal administration (tablet) |
|
| Immediate release morphine | Active Comparator | Immediate release morphine, solution Dosage: Start with a minimum of 5mg (to be determined by titration) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Fentanyl | Drug |
|
| |
| Measure | Description | Time Frame |
|---|---|---|
| Time to onset of meaningful breathlessness relief | To determine the time to onset of meaningful breathlessness relief of fentanyl buccal tablet (FBT) in comparison to immediate-release morphine (IRM) | minutes (by stop watch) from drug application of FBT/IRM up to breathlessness relief |
| Measure | Description | Time Frame |
|---|---|---|
| Breathlessness intensity | Breathlessness intensity measured by NRS (range 0-10) | at 0, 3, 5, 10, 15, 20, 30, 45 and 60 minutes after application of FBT/IRM |
| Numbers of rescue medication doses | If adequate breathlessness relief was not reached after 30 min, the patient could use his standard rescue medication. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of (serious) adverse events (AE/SAE; Safety of FBNT/IRM) | Counts of adverse events | through study completion, day 10 (e.g. final visit) |
| Severity of AE/SAE (Safety of FBNT/IRM) | CTCAE tool v4.03 (National Cancer Institute Common Terminology Criteria) |
Inclusion criteria:
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Raymond Voltz, Professor | Department of Palliative Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital Göttingen Center of Palliative Medicine | Göttingen | Hesse | 37075 | Germany | ||
| Study Center Palliative Medicine |
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
| D004418 | Dyspnea, Paroxysmal |
| ID | Term |
|---|---|
| D004417 | Dyspnea |
| D012120 | Respiration Disorders |
| D012140 | Respiratory Tract Diseases |
| D006333 | Heart Failure |
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| ID | Term |
|---|---|
| D005283 | Fentanyl |
| ID | Term |
|---|---|
| D010880 | Piperidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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| Immediate release morphine |
| Drug |
|
|
| Numbers of rescue medication doses through study completion, assessed at day 10 (final visit) |
| Patient's & investigator's satisfaction | Patient's and investigator's satisfaction of breathlessness relief and route of application regarding ease of administration (4-point verbal rating scale: 0 = poor/unsatisfied and 4 = excellent/very satisfied). | through study completion, day 10 (e.g. final visit) |
| Preferences of study drugs | FBT or IRM or both/none | through study completion, day 10 (e.g. final visit) |
| through study completion, day 10 (e.g. final visit) |
| Oxygen saturation (Safety of FBNT/IRM) | finger clip pulse oximetry (Contec Medical Systems Co., China) | through study completion, day 10 (e.g. final visit) |
| Patient's vigilance (Safety of FBNT/IRM) | Glasgow Coma Scale (GCS) | through study completion, day 10 (e.g. final visit) |
| Respiratory rate (Safety of FBNT/IRM) | breaths per minute | through study completion, day 10 (e.g. final visit) |
| Enrollment rate (Feasibility of study procedures) | Ratio of patients screened to patient with informed consent | day 10 (e.g. final visit) |
| Completion rate (Feasibility of study procedure) | Ratio of patients that were randomly assigned to the experimental vs active comparator arm to patients that completed the study | day 10 (e.g. final visit) |
| Drop outs (Feasibility of study procedures) | Counts of drop out per visit (TPh+EPh) | day 10 (e.g. final visit) |
| Reasons for rejection of study participation of screened patient (Feasibility of study procedures) | List of reasons/ free text responses | day 10 (e.g. final visit) |
| Acceptability of study procedures | closed questions: 4-point verbal rating scale between 0=poor/unsatisfied and 4=excellent/very satisfied, and yes/no; reports by patients, investigators and clinical team | day 10 (e.g. final visit) |
| Acceptability of measurement tools | closed questions: 4-point verbal rating scale between 0=poor/unsatisfied and 4=excellent/very satisfied, and yes/no; reports by patients, investigators and clinical team | day 10 (e.g. final visit) |
| Acceptability of rescue procedures | closed questions: 4-point verbal rating scale between 0=poor/unsatisfied and 4=excellent/very satisfied, and yes/no; reports by patients, investigators and clinical team | day 10 (e.g. final visit) |
| Cologne |
| North Rhine-Westphalia |
| 50937 |
| Germany |
| Hospital Essen- Mitte, Departement of Palliative Medicine | Essen | North Rhine-Westphalia | 45136 | Germany |
| D006331 |
| Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D012818 | Signs and Symptoms, Respiratory |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |