MedPath

Surgical wound dressing vs non dressing

Not Applicable
Conditions
Surgical intervention is studied
Registration Number
SLCTR/2009/005
Lead Sponsor
Dr. L.L.N.R.Lekamge
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow up complete
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

All the patient who gives the consent and does not fall in the exclusion criteria

Exclusion Criteria

*Patients who do not give their consent to participate *Known infection or fever at the time of surgery *Dribbling for > 24 hours *Previous hypertrophic scar or a keloid *Patients currently on antibiotics or steroids *Patient and or the surgeon preference of either method *Immune suppressed patients or any medical condition in need of addition of antibiotics *Emergency surgeries where there is not enough time to obtain informed consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Surgical site complications <br>•Wound disruption •Wound erythema •Wound discharge •Haematoma or seroma formation (To determine the occurrence of surgical site infection )<br> []<br>
Secondary Outcome Measures
NameTimeMethod
Perception of post operative pain, nursing time and cosmetic appearance after 8 weeks.<br><br> []<br>
© Copyright 2025. All Rights Reserved by MedPath