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NCT02689258 · ClinicalTrials.gov registry record · Phase 2
Evaluation of the Efficacy and Safety of HTX-011 for Postoperative Analgesia Following Abdominoplasty Surgery
A Phase 2 study, sponsored by Heron Therapeutics.
- Completed
- Registry status
- Phase 2
- Development phase
- 277
- Enrollment target
NCT02689258: Completed Phase 2 study, sponsored by Heron Therapeutics.
NCT02689258 is a Phase 2 study that has completed, run by Heron Therapeutics. The registered enrollment target is 277 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (108% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02689258, a Phase 2 study, has completed, sponsored by Heron Therapeutics.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 277 participants
- Enrollment target
Study Summary
A Phase 2, Randomized, Controlled Evaluation of the Efficacy and Safety of HTX-011 or HTX-002 for Post-Operative Analgesia Following Abdominoplasty Surgery
Primary Outcome
The SPI is derived by summing the pain intensity score weighted by the scheduled time duration. SPI0-24 will be calculated by summing the Pain intensity (PI) score at the relevant time points weighted by the scheduled time duration since the prior PI assessment as follows: SPI0-24= PI1+PI2+2\*PI4+2\*PI6+2\*PI8+2\*PI10+2\*PI12+2\*PI14+4\*PI18+6\*PI24. Min = 0 (if PI=0 at every time) and Max = 240 (if PI=10 at every time).
Interventions
- DRUG Placebo
- DRUG Bupivicaine HCl
- DRUG HTX-002
- DRUG HTX-011A
- DRUG HTX-011B
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 277 participants |
| Start Date | 2016-02-23 |
| Est. Completion | 2017-04 |
| Phase | Phase 2 |
What the finished NCT02689258 record still lists
NCT02689258 is an interventional study that assigns participants to a tested intervention. The registered 277 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (108% higher).
The record links to 0 conditions, and to 5 interventions - of which Placebo is the first listed.
NCT02689258 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02689258 about?
NCT02689258 is a clinical study titled "Evaluation of the Efficacy and Safety of HTX-011 for Postoperative Analgesia Following Abdominoplasty Surgery". A Phase 2, Randomized, Controlled Evaluation of the Efficacy and Safety of HTX-011 or HTX-002 for Post-Operative Analgesia Following Abdominoplasty Surgery
What is the current status of trial NCT02689258?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 277 participants. The study started on 2016-02-23. Estimated completion is 2017-04.
What interventions are being tested in trial NCT02689258?
The interventions under investigation include: Placebo (DRUG), Bupivicaine HCl (DRUG), HTX-002 (DRUG), HTX-011A (DRUG), HTX-011B (DRUG).
Who is sponsoring clinical trial NCT02689258?
This trial is sponsored by Heron Therapeutics, which has 23 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02689258's enrollment target sits among peer trials
277 202nd of 2000 higher than 1,799 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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