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OpenTrials
Completed

NCT Number: NCT03250221

Comparison of Robot-assisted Laparoscopic Myomectomy and Traditional Laparoscopic Myomectomy With Barbed Sutures

To elucidate the impact of barbed sutures on robotic myomectomy and laparoscopic myomectomy

Completed

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Key information

Conditions

Myomectomy

Age range

20 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Far Eastern Memorial Hospital

Banqiao District, New Taipei, 22050, Taiwan

About this study

The aim of our study will be to elucidate the impact of the use of barbed sutures on robotic myomectomy and laparoscopic myomectomy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All women who underwent robotic myomectomy and conventional laparoscopic myomectomy in the Department of Obstetrics & Gynecology of Far Eastern Memorial Hospital.

Exclusion criteria

  • Open myomectomy

Treatment and study plan

barbed sutures

Device

Use of the barbed sutures for robotic or laparoscopic myomectomy

Other names: V-Loc

Vicryl@ suture

Device

Use of Vicryl@ suture for robotic or laparoscopic myomectomy

Primary outcomes

  1. Abdominal drainage amount

    Time frame: 1 day

    Postoperative day 1 abdominal drainage amount

Secondary outcomes

  1. Blood loss

    Time frame: 1 day

    Blood loss during surgeries

  2. Surgical time

    Time frame: 1 day

    Surgical time

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Aug 15, 2017
Registry last updated
Feb 12, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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