Clinical Trial

The Effect of Uterine Manipulator Use During Abdominal Hysterectomy on Postoperative Sexual Function

Study acronym: UMAH
Recruiting
View on ClinicalTrials.gov →
Summary
This prospective, single-center, randomized controlled trial aims to evaluate the effect of uterine manipulator use during total abdominal hysterectomy on postoperative female sexual function at 3 months, assessed by the Female Sexual Function Index (FSFI). Secondary outcomes include operative time, perioperative hemoglobin change, postoperative pain (VAS), hospital stay duration, and 30-day complications.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-02-20.
Status change: Not Yet Recruiting → Recruiting 2026-03-02
Trial Details
NCT Number NCT07431788
Lead Sponsor Erkan Gol
Conditions Leiomyoma (Uterine Fibroids), Adenomyoma of Uterus, Uterine Bleeding
Enrollment 60 participants
Start Date 2026-03-02
Primary Completion 2027-02 (estimated)
Study Completion 2027-02 (estimated)
Updated on ClinicalTrials.gov 2026-03-03