Clinical Trials Logo
  1. Home
  2. Myomectomy
  3. NCT03250221
  4. Details
NCT03250221 Clinical Trial

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

Myomectomy Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03250221
Other study ID # 106024-E
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 3, 2017
Est. completion date November 1, 2017

Study information
Verified date February 2019
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 80
Est. completion date November 1, 2017
Est. primary completion date November 1, 2017
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• barbed sutures
Use of the barbed sutures for robotic or laparoscopic myomectomy
• Vicryl@ suture
Use of Vicryl@ suture for robotic or laparoscopic myomectomy

Locations
Country Name City State
Taiwan Far Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)
Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (1)

Hsiao SM, Lin HH, Peng FS, Jen PJ, Hsiao CF, Tu FC. Comparison of robot-assisted laparoscopic myomectomy and traditional laparoscopic myomectomy. J Obstet Gynaecol Res. 2013 May;39(5):1024-9. doi: 10.1111/j.1447-0756.2012.02073.x. Epub 2013 Feb 4. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Abdominal drainage amount Postoperative day 1 abdominal drainage amount 1 day
Secondary Blood loss Blood loss during surgeries 1 day
Secondary Surgical time Surgical time 1 day
See also
  Status Clinical Trial Phase
Not yet recruiting NCT04080375 - Preoperative Vaginal Dinoprostone Prior to Abdominal Myomectomy Phase 3
Completed NCT03634306 - Ultravision Visual Clearing System in Laparoscopic Hysterectomy and Myomectomy N/A
Completed NCT03308643 - Effect of Oxytocin Infusion on Blood Loss During Abdominal Myomectomy Phase 4
Recruiting NCT03363425 - Effect of Perioperative iv Dexmedetomidine vs. Lidocaine on Postoperative Pain, Analgesic Consumption and Recovery After Abdominal Gynaecological Surgery Phase 2/Phase 3
Not yet recruiting NCT04358965 - Tranexamic Acid Versus Vaginal Misoprostol in Abdominal Myomectomy Phase 4
Not yet recruiting NCT04357015 - Intravenous Tranexamic Acid Versus IV Carbetocin in Abdominal Myomectomy Phase 4
Completed NCT02741531 - The Effect of Partial Bladder Filling on Post-operative Time to Void in Minimally Invasive Gynecologic Procedures N/A
Completed NCT02049242 - Uterine Tourniquet at Open Myomectomy N/A
Completed NCT00978601 - Improved Recovery Using Multimodal Peri-operative Analgesia in Minimally Invasive Myomectomy N/A
Not yet recruiting NCT04357002 - Intravenous Tranexamic Acid Versus Vaginal Dinoprostone in Abdominal Myomectomy Phase 4
Completed NCT03892668 - Intravenous Oxytocin Versus Tranexamic Acid in Reducing Blood Loss During Abdominal Myomectomy. Phase 4