Clinical Trial

Comparing Polyglactin vs Polypropylene Sutures for Rectus Sheath Closure

Study acronym: PolySuture
Not Yet Recruiting
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Summary
This randomized controlled trial aims to compare the outcomes of Polyglactin (Vicryl) versus Polypropylene (Prolene) sutures for rectus sheath closure in patients undergoing midline laparotomy. The study will evaluate the rates of incisional hernia, surgical site infection (SSI), wound dehiscence, chronic pain, and suture sinus formation. Participants aged 18-70 years, undergoing either elective or emergency laparotomy, will be randomly assigned to receive either Polyglactin or Polypropylene sutures. The primary outcome measure is the incidence of incisional hernia at 6 months, with secondary outcomes including SSI, wound complications, and chronic pain. The study is particularly important in the context of Pakistan, where such comparative data is limited, and aims to provide evidence-based recommendations for optimal suture material selection in general surgery.
Trial Details
NCT Number NCT07280975
Lead Sponsor Lady Reading Hospital, Pakistan
Conditions Chronic Pain, Wound Dehiscence, Surgical Site Infection (SSI), Incisional Hernia, Rectus Sheath Closure, Abdominal Surgery
Enrollment 156 participants
Start Date 2026-04-01
Primary Completion 2027-06-30 (estimated)
Study Completion 2027-07-30 (estimated)
Updated on ClinicalTrials.gov 2025-12-15