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Study identifier: NCT07431788 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Leiomyoma (Uterine Fibroids) · Adenomyoma of Uterus · Uterine Bleeding  ·  Sponsor: Erkan Gol

PhaseNA
Planned participants60
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Erkan Göl, MD  ·  +905398517917  ·  drerkangol@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Bakirkoy Dr. Sadi Konuk Training and Research HospitalIstanbul, Istanbul, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07431788