drugset / Trial / NCT04175509

Improving Post-Operative Pain and Recovery in Gynecologic Surgery

NCT04175509 ↗

Phase 4 Completed 40 enrolled Aultman Health Foundation
RandomizedParallel-groupSingle-blindSupportive care

Summary

This is a clinical investigation to determine the efficacy of rectal versus intravenous acetaminophen in patients undergoing a minimally invasive hysterectomy. All women will receive acetaminophen either rectally or intravenously immediately postoperative, prior to extubation. Patient's will be randomly assigned to either the rectal acetaminophen or the intravenous acetaminophen group. Patient outcomes will be measured through a Numeric Rating Scale (NRS) from 0-10 for pain scores, and total opioid consumption measured in morphine milligram equivalent (MME) for the first 24 hours following surgery, or upon discharge, whichever comes first.

Timeline

Start
2019-12-23
Primary completion
2021-06-01
Completion
2021-06-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Acetaminophen Small molecule 1000 mg Rectal
Comparator Acetaminophen Small molecule 1300 mg Rectal

Indications

No indication recorded.