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Clinical Trial Summary

The goal of this study is to evaluate the efficacy and safety of combined CO2 fractional laser with Bimatoprost 0.03% as novel treatment of alopecia areata. The main question to study is will the bimatoprost facilitate hair growth if added to fractional CO2 laser treatment in Alopecia areata.


Clinical Trial Description

The study included 30 patients who were diagnosed clinically and dermoscopically as alopecia areata with age ranged between 16-55 years. The patients are divided into 2 groups: Group I, received fractional laser sessions with immediate and daily Bimatoprost application and Group II, received only frequent Laser sessions. Laser sessions were given to each patch once every 3 weeks, the procedure was repeated for 3 times. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05600673
Study type Interventional
Source Al-Azhar University
Contact
Status Completed
Phase Phase 1/Phase 2
Start date January 1, 2019
Completion date May 1, 2021

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