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

Inclusion Criteria5

  • Female ≥ 18 years of age at time of surgery
  • English or Spanish-speaking
  • Documentation of pelvic organ prolapse as evidenced by Stage 2, 3, or 4 prolapse on preoperative Pelvic Organ Prolapse Quantification system (POP-Q) examination
  • Surgery to be performed by a urogynecologist
  • Ambulatory or inpatient surgery acceptable

Exclusion Criteria10

  • Mesh-augmented prolapse repair (robotic, laparoscopic, or open sacrocolpopexy or sacrohysteropexy, vaginal mesh)
  • Urogynecologic surgery without prolapse repair (i.e. midurethral sling, intravesicular botox, hysterectomy only)
  • Suspected genital herpes simplex virus (HSV), molluscum contagiosum virus (MCV), condyloma acuminata, or vulvar/vaginal skin and soft tissue infection at recruitment by patient report
  • Daily opioid use (short or long-acting)
  • Concurrent non-urogynecologic surgery (i.e. rectopexy, staging or debulking for malignancy)
  • Lack of access to operative report
  • Pregnant (as determined by positive urine pregnancy test on the day of surgery via standard testing or current pregnancy documented in the preoperative note)
  • Incarcerated
  • Unable to give consent/conserved
  • Unable to complete study intervention or assessment per investigators

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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

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NCT07215780


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