Intraperitoneal Infusion of Analgesic for Postoperative Pain Management

Recruiting now · Phase 4

Conditions studied: Hysterectomy, Gynecologic Surgical Procedures, Narcotic Use, Pain, Postoperative

In brief

The study is a prospective, double-blinded, placebo-controlled multi-center trial to measure if postoperative pain and the amount of narcotics used are reduced by a clinically significant amount in women undergoing minimally invasive hysterectomy receiving a continuous infusion of intraperitoneal (IP) local anesthetic (LA) or a continuous infusion of LA combined with an NSAID compared with a control group who receives only 0.9% normal saline.

Key facts

Study ID
NCT04130464
Run by
Ying Liu
People needed
120
Starts
2019-09-30
Expected to finish
2026-12-01
Last updated by the study team
2026-04-09

Who can join

Age: 18 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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