RecruitingNot ApplicableNCT07215780

SORE Study: Sitz Baths After Urogynecologic Reconstruction


Sponsor

Yale University

Enrollment

112 participants

Start Date

Oct 28, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the utility of postoperative sitz baths in patient pain perception and recovery following surgical repair of prolapse. The SORE Study is a prospective, randomized controlled trial that aims to compare postoperative pain intensity one week after native tissue repair of pelvic organ prolapse for patients undergoing a sitz bath regimen versus usual care. Findings from this study may contribute to more robust, multimodal postoperative pain management plans if proven efficacious or, alternatively, reduce plastic medical waste and simplify postoperative pain plans if found to be ineffective.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Sitz Bath for people with gynecologic surgeries, postoperative pain management, and other related conditions. The study is currently recruiting participants at 4 locations. People eligible for this study include women aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICESitz Bath

Warm water sitz bath, 7 nights, 10 minutes each


Locations(4)

Bridgeport Hospital

Bridgeport, Connecticut, United States

Greenwich Hospital

Greenwich, Connecticut, United States

Yale-New Haven Hospital

New Haven, Connecticut, United States

Lawrence + Memorial Hospital

New London, Connecticut, United States

View Full Details on ClinicalTrials.gov

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NCT07215780


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