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Study identifier: NCT04130464 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Intraperitoneal Infusion of Analgesic for Postoperative Pain Management

Condition: Hysterectomy · Gynecologic Surgical Procedures · Narcotic Use  ·  Sponsor: Ying Liu

PhasePhase 4
Planned participants120
Who can joinFemale, 18 Years to 65 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Radwa Aly  ·  202 677 6209  ·  raly@mfa.gwu.edu

Always discuss trial participation with your own doctor first.

Locations (2)

MedStar Washington Hospital CenterWashington D.C., District of Columbia, United StatesRecruiting
The GW Medical Faculty AssociatesWashington D.C., District of Columbia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04130464