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Skin Staples Versus Polypropylene for Skin Closure in Elective Laparotomy: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 15
Maximum Age: 50
Healthy Volunteers: t
View:

• Age 15-50 years Elective laparotomy ASA I-III Written informed consent Male or female

Locations
Other Locations
Pakistan
Pakistan Institute of Medical Sciences
RECRUITING
Islamabad
Time Frame
Start Date: 2026-01-31
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 130
Treatments
Experimental: Skin Staples
Skin closure performed using disposable stainless steel skin staples.
Active_comparator: Poly propylene sutures
Skin closure performed using interrupted polypropylene (Prolene) sutures.
Related Therapeutic Areas
Sponsors
Leads: Pakistan Institute of Medical Sciences

This content was sourced from clinicaltrials.gov