Postoperative Opioid Consumption After Urogyneocologic Surgery

Completed · Not applicable

Conditions studied: Pelvic Organ Prolapse

In brief

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.

Key facts

Study ID

NCT03586219

Run by

University of California, Irvine

People needed

146

Starts

2017-12-29

Expected to finish

2020-11-28

Last updated by the study team

2021-04-15

Who can join

Age: 18 and older, up to 99. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female
• Age 18-99 years old
• English speaking
• Evaluated by a provider within the Urogynecology division at UC Irvine Medical Center, Kaiser Permanente Orange County - Irvine Medical Center, or Kaiser Permanente Orange County - Anaheim Medical Center, and consented for either a uterosacral ligament suspension, sacrospinous ligament fixation, minimally-invasive colpopexy (either laparoscopic or robotic-assisted laparoscopic), colporrhaphy, or colpocleisis

You may not qualify if…

• Non English-speaking
• Cognitive deficits that would prevent the patient from completing the study questionnaires
• Cancellation of the surgery
• Combined case with another surgical service (i.e. colorectal surgery)

Where it is running

• Kaiser Permanente Orange County - Anaheim — Anaheim, California, United States
• Kaiser Permanente Orange County-Irvine Medical Center — Irvine, California, United States
• University of California Irvine Medical Center — Orange, California, United States

Full record on ClinicalTrials.gov

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