None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Individuals aged more than 18 years Patients with clinically diagnosed keloid scars confirmed by history and examination Willingness to avoid other scar treatments during the study period Ability to give written informed consent
Exclusion criteria
Exclusion criteria: Active infection or ulceration over or around the keloid site History of keloid treatment within the past 3 months eg steroid injections, laser, cryotherapy Patients on systemic steroids, immunosuppressants, or anticoagulants Pregnant or lactating women Known hypersensitivity or allergy to pirfenidone or laser procedures. History of hypertrophic scars or other dermatological conditions mimicking keloids. Patient with systemic diseases affecting wound healing uncontrolled diabetes, autoimmune disease Patients with unrealistic expectations HIV, Hepatitis C, Hepatitis B positive patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in keloid size , symptomatic relief and scar appearance Timepoint: assessment after 4 weeks , 8 weeks . 12 weeks , 16 weeks , 20 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Jawaharlal Nehru Medical College , Datta Meghe Institute Of Higher Education And Research ,