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Intraperitoneal Infusion of Analgesic for Postoperative Pain Management

RecruitingPhase 4Healthy volunteers welcome

The Impact of the Continuous Infusion of Intraperitoneal Analgesics on Postoperative Pain After Minimally Invasive Hysterectomy: a Randomized Controlled Trial

Who can join

Ages 18 to 65 · Women · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* Hysterectomy planned for a benign gynecologic reason (no evidence of, or concern for, malignancy in the cervix, uterus, tubes or ovaries. Benign gynecologic reasons to have a hysterectomy include fibroids, abnormal uterine bleeding, endometriosis, and pelvic pain.)
* Patient is scheduled to have surgery with a fellowship trained minimally invasive gynecologic surgeons at one of the study sites.
* Patient is planned for a robotic assisted total laparoscopic hysterectomy (RA-TLH) or a total laparoscopic hysterectomy (TLH).
* Patient is capable of informed consent.
* Patient is capable of completing the questionnaires.

Exclusion Criteria:

* Concern for malignancy
* The procedure is scheduled outside MIGS department.
* Allergy to any study related medication (i.e. Ketorolac and Ropivacaine)
* Patient is enrolled in another pain management study.

About the 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.

What is being tested

Sponsor: Ying Liu · Participants: 120 · Started: Sep 30, 2019

Contact the study team

Official record on ClinicalTrials.gov — NCT04130464

Locations in the U.S.

District of ColumbiaMedStar Washington Hospital Center, Washington D.C.
The GW Medical Faculty Associates, Washington D.C.

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.