drugset / Trial / NCT06379425

Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries

NCT06379425

Phase 4 Recruiting 70 enrolled Northwell Health
RandomizedCrossoverOpen-labelPrevention

Summary

This is a double-arm randomized control trial evaluating the impact of preoperative opioid-free analgesia on time to trial of void in ambulatory urogynecologic surgeries. The investigators hypothesize that receipt of acetaminophen, celecoxib and gabapentin preoperatively versus acetaminophen alone will reduce the time to trial of void in patients undergoing same-day minor urogynecologic procedures.

Timeline

Start
2024-03-01
Primary completion
2026-03-01
Completion
2026-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Celecoxib Other / unclassified 400 mg Oral
Subject Gabapentin Small molecule 300 mg Oral
Background Acetaminophen Small molecule 1000 mg Oral

Indications

No indication recorded.