Clinical Outcomes of Robotic Myomectomy

Recruiting

• Conditions: Women With Uterine Myoma

• Registration Number: NCT06208891
• Lead Sponsor: Far Eastern Memorial Hospital

Brief Summary

To identify the predictors of perioperative outcomes in women who receive robotic myomectomy

Detailed Description

Uterine myoma is the most common gynecological tumor. Current surgical management was inclusive of conventional abdominal myomectomy, laparoscopy-assisted myomectomy, robotic-assisted myomectomy. The aim of this study was to identify the predictors of perioperative outcomes in women who receive robotic myomectomy

Study Timeline

• Study Start: 2023-11-21
• Status Verified: 2023-12
• Study First Submitted: 2023-12-05
• Study First Submitted QC: 2024-01-05
• Last Update Submitted: 2024-01-05
• Study First Posted: 2024-01-17
• Last Update Posted: 2024-01-17
• Primary Completion: 2024-12-31
• Study Completion: 2024-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: Female
• Target Recruitment: 400

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Surgical time	1 week	Factors (e.g., the location and largest diameter of the uterine myoma) predicting surgical time

Secondary Outcome Measures

Name	Time	Method
Intraoperative blood loss	1 week	Factors (e.g., the location and largest diameter of the uterine myoma) predicting intraoperative blood loss

Trial Locations

Locations (1)

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