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Clinical Trials/NCT07142395
NCT07142395
Completed
Not Applicable

Comparison of Primary Skin Closure Versus Delayed Primary Skin Closure in Patients Undergoing Emergency Laparotomies

Bkahtawar Amin Medical and Dental College Multan1 site in 1 country82 target enrollmentStarted: May 16, 2025Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Bkahtawar Amin Medical and Dental College Multan
Enrollment
82
Locations
1
Primary Endpoint
Wound Infection

Overview

Brief Summary

The purpose of this study is to find out which type of wound closure after emergency abdominal surgery leads to fewer wound infections and better recovery: closing the wound immediately after surgery (called primary closure) or waiting a few days before closing the skin (called delayed primary closure).

Wound infection is a common problem after emergency abdominal surgery (also called laparotomy). Some surgeons close the skin right away, while others wait a few days to reduce the risk of infection.

This study will help find out which method is better.

The main questions the study aims to answer are:

  1. . Does delayed primary closure lower the rate of wound infection compared to primary closure?
  2. . Does the wound open up (wound dehiscence) less often with delayed closure?
  3. . Does delayed closure affect the length of hospital stay?

In this clinical trial:

  • Adult patients needing emergency abdominal surgery will be included.
  • Half the patients will have their wounds closed immediately (primary closure), and half will have delayed closure after 3-5 days of daily dressing.
  • All surgeries will be done by experienced surgeons using the same technique.
  • Patients will be followed for 4 weeks after surgery to monitor wound infection, wound opening, and length of hospital stay.

The results will help doctors choose the safest and most effective way to close surgical wounds after emergency abdominal surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients 18 - 60 years of age
  • Either male or female gender and
  • Planned to undergo emergency laparotomy

Exclusion Criteria

  • Patients undergoing second laparotomy
  • Re- laparotomy
  • On steroid therapy and
  • Patients who die within 28-days of surgery

Outcomes

Primary Outcomes

Wound Infection

Time Frame: From date of surgery to Four weeks postoperatively

Surgical Site infection - Presence any features of erythema, pain, pus discharge on examination of surgical wound and new onset fever (\> 98.6 F)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Bkahtawar Amin Medical and Dental College Multan
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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