A study to observe the effects of a treatment option for acne scars
Not Applicable
- Conditions
- Health Condition 1: L705- Acne excorieeHealth Condition 2: L700- Acne vulgarisHealth Condition 3: L709- Acne, unspecifiedHealth Condition 4: L909- Atrophic disorder of skin, unspecifiedHealth Condition 5: L708- Other acneHealth Condition 6: L908- Other atrophic disorders of skinHealth Condition 7: L905- Scar conditions and fibrosis of skin
- Registration Number
- CTRI/2024/05/067801
- Lead Sponsor
- Dr Silpa Rajesh Raj
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients diagnosed with acne scarring aged 18 years or above are included.
Exclusion Criteria
Those with known photosensitivity, pregnancy, lactation, keloidal tendency, use of oral retinoids in last 6 months, infections like herpes labialis and history of pacemaker implantation are excluded.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the improvement of facial acne scars qualitatively, quantitatively and subjectively in terms of percentages. To monitor the various side effects that can occur during the procedure.Timepoint: Monthly for 4 months
- Secondary Outcome Measures
Name Time Method To monitor the various side effects that can occur during the procedure.Timepoint: Monthly for 4 months