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Clinical trialNCT07215780RecruitingInterventional

SORE Study: Sitz Baths After Urogynecologic Reconstruction

SponsorYale UniversityEnrollment112Gynecologic SurgeriesPelvic Organ ProlapsePostoperative Pain Management
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Bridgeport Hospital

    Bridgeport, Connecticut, United States

    Recruiting
  • Greenwich Hospital

    Greenwich, Connecticut, United States

    Recruiting
  • Yale-New Haven Hospital

    New Haven, Connecticut, United States

    Recruiting
  • Lawrence + Memorial Hospital

    New London, Connecticut, United States

    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
28 Oct 2025
Primary completion
31 Mar 2027
Completion
30 Jun 2027
Last update posted
3 Dec 2025
Registered enrollment
112
Registry id
NCT07215780

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.