Clinical Trial

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

Recruiting Phase 4
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Record status
This record was last updated May 22, 2025 (before its estimated March 1, 2026 completion). Its status may not reflect the trial's current state.
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-04-17.
Trial Details
NCT Number NCT06379425
Lead Sponsor Northwell Health
Conditions Pain, Postoperative, Postoperative Pain, Acute
Enrollment 70 participants
Start Date 2024-03-01
Primary Completion 2026-03-01 (estimated)
Study Completion 2026-03-01 (estimated)
Updated on ClinicalTrials.gov 2025-05-22