Clinical Trial

SORE Study: Sitz Baths After Urogynecologic Reconstruction

Study acronym: SORE
Recruiting
View on ClinicalTrials.gov →
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.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-10-08; most recent amendment 2025-11-25.
Status change: Not Yet Recruiting → Recruiting 2025-10-15
Trial Details
NCT Number NCT07215780
Lead Sponsor Yale University
Collaborators: American Urogynecologic Society
Conditions Pelvic Organ Prolapse, Postoperative Pain Management, Gynecologic Surgeries
Enrollment 112 participants
Start Date 2025-10-28
Primary Completion 2027-03 (estimated)
Study Completion 2027-06 (estimated)
Updated on ClinicalTrials.gov 2025-12-03