Monitoring improvement of acne scars after treatment with Erbium laser.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Acne Scars
- Registration Number
- CTRI/2018/06/014433
- Lead Sponsor
- DR PREETHI JOLLY
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Patients willing for the study.
Patients more than 18 years of age.
All the patients presenting with moderate to severe acne scarring.
Patients who have not taken retinoids in the last 3 months.
Exclusion Criteria
Patients who are not willing for the study.
Pregnant or lactating women.
Patients with history of developing hypertrophic scars or keloids.
Extensive active acne lesions or with secondary infection.
Patients with concurrent herpes simplex infection.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction of acne scars.Timepoint: Reduction of acne scars after one month of each session (4 sessions in total).
- Secondary Outcome Measures
Name Time Method Pain during session and post inflammatory pigmentation.Timepoint: To be assessed one month after each session (4 sessions in total)