Health Condition 1: L700- Acne vulgaris
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.All patients of age more than 18 years of both the genders who are diagnosed and classified as atrophic Acne scar clinically. 2. Patients who have given consent for the study. 3. Patients who are willing to come for regular
Exclusion criteria
Exclusion criteria: 1.Pregnant and lactating women. 2.Patients taking oral contraceptive pills or hormonal replacement therapy at the time of study or during the past 12 months. 3.Concomitant use of anticoagulants or Patients with history of bleeding diathesis. 4.Patients with history of hypertrophic scar & keloids. 5.Active skin infection in the area of acne scar. 6.History of photosensitivity.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of monotherapy versus combination therapy in the treatment of atrophic acne scar.Outcome will be assessed at baseline(0),4,8 and12 weeks and at the end of 3rd month after last sitting using Goodman and Baron qualitative acne scar score. Timepoint: To compare the efficacy of monotherapy versus combination therapy in the treatment of atrophic acne scar.Outcome will be assessed at baseline(0),4,8 and12 weeks and at the end of 3rd month after last sitting using Goodman and Baron qualitative acne scar score. | — |
Secondary
| Measure | Time frame |
|---|---|
| To analyse the number of sessions needed for the visual improvement, sustainability of results & safety outcomes in a patient with atrophic acne scar.Outcome will be assessed at baseline(0week),4,8,12th week & at the end of 3rd month after last sittingTimepoint: Physician will be Scored as Bad,Good And Excellent using visual improvementscale.Outcome will be assessed at baseline(0week),4,8,12th week & at the end of 3rd month after last sitting | — |
Countries
India
Contacts
Madras medical college and hospital,RGGGH