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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 is a NA study that has completed, run by University of California, Irvine. The registered enrollment target is 146 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03586219
The ClinicalTrials.gov registry entry for NCT03586219 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 146 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Irvine, which has 368 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Opioid-specific educational patient pamphlets is the first listed.
NCT03586219 reports 0 study locations.
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.
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