NCT04785404CompletedNot Applicable
Primary Versus Secondary Closure of Stoma-Reversal Skin Wound: Randomized Controlled Trial
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Ayub Teaching Hospital
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- surgical site infection
Study Overview
Brief Summary
to compare infection rate stoma reversal skin wound after primary or secondary closure
Detailed Description
There will be two groups. In group A, skin will be stitched with prolene while in group B skin will be left open to follow up till 1 month and wound observed for infection according to CDC guidelines.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •. All patients who undergo ileostomy or colostomy reversal will be included
Exclusion Criteria
- •included patients with reversal of stoma through laparatomy, post-operative anastomotic leak and co-morbidities like diabetes, Chronic liver disease, chronic kidney disease etc
Arms & Interventions
primary skin closure
Experimental
in this group, skin wound will be primarily closed
Intervention: primary skin closure (Procedure)
secondary skin closure
No Intervention
skin will be left open to heal by secondary intention
Outcomes
Primary Outcomes
surgical site infection
Time Frame: 30 days
skin wound infection at surgical site will be observed on CDC guidelines
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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