FMRF Combined With 30% SSA in the Treatment of Rosacea
Status:
COMPLETED
Trial end date:
2024-11-14
Target enrollment:
Participant gender:
Summary
This study was a single-center, case-by-case, bilateral facial comparison study. A total of 15 patients were included. On the day of enrollment, after the completion of the test items, treatment was carried out (full face gold micro-needling + 30% salicylic acid on the half face), and on-site follow-up was conducted 1 week later, 2 weeks later follow-up was conducted and the second acid brushing treatment was performed, 4 weeks later follow-up was conducted and the third acid brushing treatment was performed, on-site follow-up was conducted at the 8th week and the 12th week, and the follow-up contents included: Visia photography, camera photography, non-invasive skin testing, questionnaire assessment, etc. The study duration was 12 weeks.
Phase:
NA
Details
Lead Sponsor:
Second Affiliated Hospital of Xi'an Jiaotong University