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NCT03586219 · ClinicalTrials.gov registry record · NA
Postoperative Opioid Consumption After Urogyneocologic Surgery
A NA study, sponsored by University of California, Irvine.
- Completed
- Registry status
- NA
- Development phase
- 146
- Enrollment target
NCT03586219: Completed NA study, sponsored by University of California, Irvine.
NCT03586219 is a NA study that has completed, run by University of California, Irvine. The registered enrollment target is 146 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03586219, a NA study, has completed, sponsored by University of California, Irvine.
- COMPLETED
- Registry status
- NA
- Development phase
- 146 participants
- Enrollment target
Study Summary
The purpose of this randomized controlled trial is to evaluate whether preoperative opioid education will reduce postoperative opioid consumption after urogynecologic surgeries. Additionally, the effect of the opioid education on opioid storage and disposal patterns will be evaluated. The pattern of opioid consumption 2 and 6 weeks after surgery will be compared between patients in the study arms. The rates of prescription refills 12 weeks and 12 months after the surgery will be compared between patients in the study arms.
Primary Outcome
Mean number of opioid tablets consumed 2 weeks postoperatively
Interventions
- BEHAVIORAL Opioid-specific educational patient pamphlets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 146 participants |
| Start Date | 2017-12-29 |
| Est. Completion | 2020-11-28 |
| Phase | NA |
What the finished NCT03586219 record still lists
NCT03586219 is an interventional study that assigns participants to a tested intervention. The registered 146 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 1 intervention - of which Opioid-specific educational patient pamphlets is the first listed.
NCT03586219 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03586219 about?
NCT03586219 is a clinical study titled "Postoperative Opioid Consumption After Urogyneocologic Surgery". The purpose of this randomized controlled trial is to evaluate whether preoperative opioid education will reduce postoperative opioid consumption after urogynecologic surgeries. Additionally, the effect of the opioid education on opioid storage and disposal patterns will be evaluated. The pattern of...
What is the current status of trial NCT03586219?
This trial is currently completed. It is a NA study. The enrollment target is 146 participants. The study started on 2017-12-29. Estimated completion is 2020-11-28.
What interventions are being tested in trial NCT03586219?
The interventions under investigation include: Opioid-specific educational patient pamphlets (BEHAVIORAL).
Who is sponsoring clinical trial NCT03586219?
This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03586219's enrollment target sits among peer trials
146 704th of 2000 higher than 1,296 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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