Clinical Outcome of Laparoscopic or Robotic Metroplasty for Uterine Isthmocele

Completed

• Conditions: Laparoscopic or Robotic Metroplasty

• Registration Number: NCT04414670
• Lead Sponsor: Far Eastern Memorial Hospital

Brief Summary

To evaluate the clinical outcomes of conventional or robotic - laparoscopic metroplasty for uterine isthmocele with the aid of a bending probe.

Detailed Description

Not available

Study Timeline

• Study Start: 2020-02-17
• Study First Submitted: 2020-05-31
• Study First Submitted QC: 2020-06-02
• Study First Posted: 2020-06-04
• Primary Completion: 2021-09-08
• Study Completion: 2021-11-29
• Status Verified: 2022-02
• Last Update Submitted: 2022-08-14
• Last Update Posted: 2022-08-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 20

Inclusion Criteria

• > 20 years of women
• uterine isthmocele status post laparoscopic or robotic metroplasty with a bent uterine sound

Exclusion Criteria

• Those underwent traditional open surgery.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Change of prolonged menstrual bleeding condition	10 years	Symptoms improvement and perioperative complications

Secondary Outcome Measures

Name	Time	Method
Change of scar defect size	10 years	Symptoms improvement and perioperative complications

Trial Locations

Locations (1)

Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital; 🇨🇳 Banqiao, New Taipei, Taiwan