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Postoperative Opioid Consumption After Urogyneocologic Surgery

NCT03586219 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 146

Last updated 2021-04-15

No results posted yet for this 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.

Conditions

  • Pelvic Organ Prolapse

Interventions

BEHAVIORAL

Opioid-specific educational patient pamphlets

See prior description

Sponsors & Collaborators

  • Kaiser Permanente

    collaborator OTHER

  • University of California, Irvine

    lead OTHER

Principal Investigators

  • Kristen Buono, MD · University of California, Irvine

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-29
Primary Completion
2020-11-28
Completion
2020-11-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03586219 on ClinicalTrials.gov