Scar Clinical Trial
Official title:
Comparitive Study of Efficacy and Safety Between Fractional Er:YAG Laser and Bipolar Radiofrequency Treatment for Acne Scar
Verified date | October 2013 |
Source | Seoul National University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Korea: Institutional Review Board |
Study type | Interventional |
Compare the efficacy of frational Er:YAG laser and that of bipolar frequency with diode laser treatment.
Status | Completed |
Enrollment | 27 |
Est. completion date | May 2013 |
Est. primary completion date | May 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 19 Years to 40 Years |
Eligibility |
Inclusion Criteria: - moderate acne scar Exclusion Criteria: - taking steroids, nonsteroidal antiinflammatory drug, and isotretinoin - anyone who received acne scar procedures within 6 months - underlying diabetes mellitus, keloid, or malignancy |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Department of Dermatology, Seoul National University College of Medicine | Seoul |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Hospital |
Korea, Republic of,
Kutlubay Z, Gokdemir G. Treatment of atrophic facial acne scars with the Er:YAG laser: a Turkish experience. J Cosmet Laser Ther. 2010 Apr;12(2):65-72. doi: 10.3109/14764171003706141. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Global asessment of acne scar | 5 point grading of acne scar | 12 weeks | No |
Secondary | ECCA | quantative assessement of acne scar | 12 weeks | No |
Secondary | adverse effect assessment | adverse effect assessment | 12 weeks | Yes |
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