Trials / Recruiting
RecruitingNCT07431788
The Effect of Uterine Manipulator Use During Abdominal Hysterectomy on Postoperative Sexual Function
A Prospective Randomized Controlled Trial Evaluating the Impact of Uterine Manipulator Use During Total Abdominal Hysterectomy on Postoperative Female Sexual Function
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Erkan Gol · Other Government
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Uterine Manipulator | Use of a uterine manipulator during total abdominal hysterectomy. |
| PROCEDURE | Conventional Abdominal Hysterectomy | Total abdominal hysterectomy without uterine manipulator. |
Timeline
- Start date
- 2026-03-02
- Primary completion
- 2027-02-01
- Completion
- 2027-02-01
- First posted
- 2026-02-25
- Last updated
- 2026-03-03
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT07431788. Inclusion in this directory is not an endorsement.