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Clinical Trial Summary

The objective of this study is to examine photos of CCCA patients taken before and after treatment to compare treatment outcomes between different treatment groups


Clinical Trial Description

Treatment groups that patients will be randomized to include 1) topical steroid plus oral antibiotic group, and topical minoxidil after 8 months 2) topical steroid plus intralesional steroid group and topical minoxidil after 8 months. Both these regimens are used as the first-line treatments by clinicians. The objective of this study is to examine photos of CCCA patients taken before and after treatment to compare treatment outcomes between different treatment groups. In this study, the investigators are looking to determine how standard treatment affects the outcome of central centrifugal cicatricial alopecia; to determine if topical steroid with With Doxycycline has better outcome than topical steroids with intralesional steroids in central centrifugal cicatricial alopecia, and to determine how the addition of topical minoxidil as a treatment changes the outcome of central centrifugal cicatricial alopecia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04207931
Study type Interventional
Source Wake Forest University Health Sciences
Contact Amy J McMichael, MD
Phone 336.716.3926
Email amcmichael@wakehealth.edu
Status Recruiting
Phase Phase 4
Start date April 30, 2018
Completion date November 2024

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT03491267 - Study to Determine Effect of Gentle Wounding to Stimulate Hair Follicle Neogenesis Early Phase 1