Skin Staples vs Polypropylene in Elective Laparotomy
NCT: NCT07781878 · RECRUITING
Brief Summary
Surgical site infection (SSI) is one of the most common postoperative complications following elective laparotomy and contributes significantly to patient morbidity, prolonged hospital stay, and increased healthcare costs. Various techniques are available for skin closure, including skin staples and polypropylene sutures; however, evidence regarding their comparative effectiveness remains inconsistent, particularly in low- and middle-income countries. This randomized controlled trial aims to compare skin staples with polypropylene sutures for skin closure following elective laparotomy. Eligible adult patients undergoing elective laparotomy at the Department of General Surgery, Pakistan Institute of Medical Sciences (PIMS), Islamabad, will be randomly allocated in a 1:1 ratio to receive either skin staples or polypropylene sutures. The primary outcomes are skin closure time and incidence of surgical site infection within 30 days of surgery. Secondary outcomes include wound dehiscence, postoperative pain, cosmetic scar appearance, patient satisfaction, and duration of hospital stay. The findings will provide evidence regarding the optimal skin closure technique for elective laparotomy in the Pakistani population.
Frequently Asked Questions
What is Skin Staples vs Polypropylene in Elective Laparotomy?
Skin Staples vs Polypropylene in Elective Laparotomy is a clinical trial registered under NCT07781878. Current status: RECRUITING.
What is the status of NCT07781878?
The current status of NCT07781878 (Skin Staples vs Polypropylene in Elective Laparotomy) is: RECRUITING.
When did Skin Staples vs Polypropylene in Elective Laparotomy start?
Skin Staples vs Polypropylene in Elective Laparotomy started on 2026-01-31.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.