A randomized study comparing skin closure in benign gynecologic surgery : Staple versus subcuticular suture

• Conditions: Postoperative pain; benign gynecologic surgery; Anaesthesiology - Pain management; Surgery - Surgical techniques; Reproductive Health and Childbirth - Other reproductive health and childbirth disorders

• Registration Number: ACTRN12611000399998
• Lead Sponsor: Khon Kaen Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-04-15
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: 110

Inclusion Criteria

Scheduled to undergo benign gynecologic surgery
-Performing Pfannenstiel incision

Exclusion Criteria

-Previous pfannenstiel incision
-Malignant condition

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain by using visual analog scale (VAS)[At two months after randomization]

Secondary Outcome Measures

Name	Time	Method
Wound infection by medical record at 30 days after the procedure.[At one month after randomization];Satisfaction of patient by using Patient Satisfaction Questionnaire (PSQ)[At one month after randomization]