About this trial
This randomized controlled study aims to evaluate the effects of skin closure using surgical staplers compared with conventional skin sutures on postoperative pain and wound healing in primiparous women undergoing episiotomy repair after vaginal delivery.
Primiparous women who require episiotomy during vaginal birth will be randomly assigned to one of two groups: skin closure with staples or skin closure with sutures. Postpartum pain levels and wound healing outcomes will be assessed and compared between the two groups.
The results of this study are expected to contribute to evidence-based decisions regarding optimal skin closure techniques in episiotomy repair.
Eligibility criteria
Qualifiers
Age ≥ 18 years
Term pregnancy (≥ 37 weeks)
Low-risk pregnancy (no obstetric risk factors)
Not receiving oxytocin induction during latent or active labor
Disqualifiers
Apgar score < 7 at 1 minute and/or 5 minutes
Neonatal anomaly
Use of >10 mL analgesic during episiotomy repair beyond routine practice
Obesity
Trial design
Treatments tested in this trial
- stapler skin closure
- absorbable suture group
Treatment groups
Sponsors and collaborators
Ayşegül Kanık
Lead sponsor
Ege University
Sponsor institution