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NCT04785404 Clinical Trial

Primary Versus Secondary Closure of Stoma-Reversal Skin Wound

Wound Infection Clinical Trial

Official title:
Primary Versus Secondary Closure of Stoma-Reversal Skin Wound: Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04785404
Other study ID # AyubTH
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2020

Study information
Verified date July 2021
Source Ayub Teaching Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to compare infection rate stoma reversal skin wound after primary or secondary closure

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.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• primary skin closure
skin will be stitched after stoma reversal to heal by primary intention

Locations
Country Name City State
Pakistan Ayub teaching hospital Abbottabad Khyber Pakhtunkhwa

Sponsors (1)
Lead Sponsor Collaborator
Ayub Teaching Hospital

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary surgical site infection skin wound infection at surgical site will be observed on CDC guidelines 30 days
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