Randomized controlled trial comparing Monocryl ® and Vicryl rapide ® for the subcuticular skin repair after episiotomy.

Completed

• Conditions: Episiotomy; 10036411

• Registration Number: NL-OMON35717
• Lead Sponsor: Ikazia Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 250

Inclusion Criteria

primiparous
uncomplicated episiotomy
Informed consent

Exclusion Criteria

multiparous women
vaginal or perineal laceration other than extension of the vaginal part of the episiotomy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Primary outcome is the pain score in sitting position (Visual Analogous Scale,<br /><br>VAS) 10 days postpartum</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secundary outcomes are pain (VAS-score) 24 hours postpartum, dyspareunia 10<br /><br>days postpartum and pain and dyspareunia 6 weeks and 3 months postpartum and<br /><br>complications like wound dehiscence and infection. </p><br>