CTRI/2019/08/020572
Completed
Phase 3
To study the efficacy of amniotic membrane as an alternative wound dressing in patients with large posttraumatic raw area at level 1 Trauma Centerâ??
INSTITUTE RESEARCH GRANT0 sites60 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: T07- Unspecified multiple injuries
- Sponsor
- INSTITUTE RESEARCH GRANT
- Enrollment
- 60
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients who require wound dressing for external superficial wounds following trauma having the wound dimension of 10x10cm or more, till the period requiring definitive coverage ie skin grafting or the flaps cover.
Exclusion Criteria
- •1\.Infected wounds
- •2\.Deep wounds \& internal wounds.
- •3\.Open fractures
- •4\.Known cases of Diabetes Mellitus.
- •5\.A skin disorder that is chronic or currently active and involves the areas to be examined in this trial.
- •6\.Patients who are immune\-compromised.
- •7\.Patients on steroids.
- •8\.Pregnancy or lactation
- •9\.Liver enzymes raised to twice the normal range
- •10\.Serum creatinine \> 1\.4 mg %
Outcomes
Primary Outcomes
Not specified
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