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Efficacy of autologous platelet rich plasma (PRP) in prevention of hypertrophic scar

Not Applicable
Conditions
Keloid and hypertrophic scar.
Registration Number
IRCT20201007048955N1
Lead Sponsor
Clinical Research Development Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

Not having diabetes
Not having autoimmune diseases
Not having thrombocytopenia(platelets below 150000)
Not receiving glucocorticoids

Exclusion Criteria

Patient not referring to the doctor for surveillance
Death of the patient during the surveillance period

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hypertrophic scar score. Timepoint: 2nd, 12th and 24th weeks after surgery. Method of measurement: Vancouver scar scale(VSS).
Secondary Outcome Measures
NameTimeMethod
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