Comparison of the clinical outcomes of different donor site dressing methods in patients undergoing split thickness skin grafting.
Not Applicable
- Conditions
- Health Condition 1: L988- Other specified disorders of the skin and subcutaneous tissue
- Registration Number
- CTRI/2023/03/050560
- Lead Sponsor
- self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients aged between 18 to 70 years having donor site area ranging from 2% to 80% total body surface area on their either thigh and dressed with either of the folllowing dressing materials- chlorhexidine tulle gras dressing, collagen dressing, contact-layer silver lipido-colloid dressing, non-adhesive silver foam dressing and cadaver skin graft
Exclusion Criteria
Patients on steroids, local irradiation, malignancy, collagen vascular diseases, severe anaemia (Hb < 10gm/dl), hypoproteinaemia (total serum proteins < 6 g/dl and total serum albumin < 3.4 /dl), immunocompromise, diabetes mellitus, underlying skin disease, chronic smokers, and patients who failed to follow up for six months.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method