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NCT02241486 · ClinicalTrials.gov registry record · Phase 3
Sublingual Fentanyl and Procedural Burn Pain
A Phase 3 study, sponsored by Loyola University.
- Terminated
- Registry status
- Phase 3
- Development phase
- 2
- Enrollment target
NCT02241486: Clinical Trial Phase 3 study, sponsored by Loyola University.
NCT02241486 is a Phase 3 study that was terminated before completion, run by Loyola University. The registered enrollment target is 2 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02241486, a Phase 3 study, was terminated before completion, sponsored by Loyola University.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 2 participants
- Enrollment target
Study Summary
The purpose of this study is to examine the efficacy and safety of sublingual fentanyl spray (Subsys) for procedural pain (dressing changes/minor debridement) in patients with burn injury.
Primary Outcome
Patients suffering from burn injuries will receive sublingual fentanyl spray (Subsys) to address procedural pain (dressing changes/minor debridement). It will be compared with a standard treatment regimen of oral morphine. The hypothesis is that the fentanyl spray will be more effective for the treatment of procedural pain in patients with burn injury.
Interventions
- DRUG Sublingual Fentanyl Spray
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2 participants |
| Start Date | 2013-09 |
| Est. Completion | 2015-03 |
| Phase | Phase 3 |
Why NCT02241486 stopped before completion
NCT02241486 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 1 intervention - of which Sublingual Fentanyl Spray is the first listed.
NCT02241486 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02241486 about?
NCT02241486 is a clinical study titled "Sublingual Fentanyl and Procedural Burn Pain". The purpose of this study is to examine the efficacy and safety of sublingual fentanyl spray (Subsys) for procedural pain (dressing changes/minor debridement) in patients with burn injury.
What is the current status of trial NCT02241486?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 2 participants. The study started on 2013-09. Estimated completion is 2015-03.
What interventions are being tested in trial NCT02241486?
The interventions under investigation include: Sublingual Fentanyl Spray (DRUG).
Who is sponsoring clinical trial NCT02241486?
This trial is sponsored by Loyola University, which has 92 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02241486's enrollment target sits among peer trials
2 2000th of 2000 the lowest of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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