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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04207931
Other study ID # IRB00043796
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date April 30, 2018
Est. completion date November 2024

Study information

Verified date January 2024
Source Wake Forest University Health Sciences
Contact Amy J McMichael, MD
Phone 336.716.3926
Email amcmichael@wakehealth.edu
Is FDA regulated No
Health authority
Study type Interventional

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


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date November 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - African-American women, ages 18-60 years old - with a clinical diagnosis and biopsy-proven CCCA, with Central Scalp Alopecia Scale severity 1 through 4 will be included in this study - These subjects will be seen and treated in Wake Forest Baptist Health Dermatology Outpatient Clinic Exclusion Criteria: - Patients with other forms of hair loss in addition to CCCA will be excluded - Other patients to be excluded are those with other forms of inflammatory scalp disease (with the exception of mild seborrheic dermatitis) - patients who have had topical treatment for CCCA within the past 4 months (including topical steroids, topical minoxidil, or any other topical hair regrowth medication) - patients who have been on a long-term oral antibiotics for hair loss within the past year - patients who have undergone more than two rounds of intralesional steroid injections to the scalp in the past one year.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Topical steroid class I-II
applied once daily - 18 month duration of the study
Triamcinolone Acetonide
Intralesional Steroid Injection, 7.5mg/cc. max dose of 3 cc. Scalp injections will be administered every 6-8 weeks, for a total of 8 injections.
Doxycyline
oral antibiotic twice daily for 6 months
Minoxidil
5% solution or foam started after month 8

Locations

Country Name City State
United States Wake Forest Baptist Health Department of Dermatology Winston-Salem North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Wake Forest University Health Sciences The Skin of Color Society

Country where clinical trial is conducted

United States, 

References & Publications (2)

Bin Saif GA, Ericson ME, Yosipovitch G. The itchy scalp--scratching for an explanation. Exp Dermatol. 2011 Dec;20(12):959-68. doi: 10.1111/j.1600-0625.2011.01389.x. — View Citation

Sperling LC, Sau P. The follicular degeneration syndrome in black patients. 'Hot comb alopecia' revisited and revised. Arch Dermatol. 1992 Jan;128(1):68-74. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Central Scalp Alopecia Photographic Scale in African American Women Photographs of the subject's scalp will be taken at baseline. This instrument is a 6-point scale that includes gradations in hair loss from normal (0) to bald scalp (5). Higher numbers denote greater hair loss. baseline
Primary Central Scalp Alopecia Photographic Scale in African American Women This instrument is a 6-point scale that includes gradations in hair loss from normal (0) to bald scalp (5). Higher numbers denote greater hair loss. Visit 4, Month 6
Secondary Hair Loss Questionnaire Questionnaire gathers the epidemiologic data about the patient's hair loss, family history of hair loss, what treatments have been tried in the past, and hair care practices.
There is no range and/or direction as this questionnaire is used to gather descriptive data.
Baseline, Visit 4, Month 6; Visit 7, Month 12; and Visit 9, Month 18-20
Secondary Dermatology Life Quality Index (DLQI) Questionnaire measures how CCCA and the symptoms associated have affected daily activities over the past week. A 5-point scale is used. It ranges from 'Very Much' to 'Not Relevant' with 'Very Much' meaning that it negatively affects their daily living and quality of life and 'Not Relevant' meaning that it has no effect on their daily living and quality of life. Visit 4, Month 6; Visit 7, Month 12; and Visit 9, Month 18-20
Secondary Last Year Dermatology Life Quality Index (LYDLQI) Questionnaire measures how CCCA and the symptoms associated have affected daily activities over the past year. A 5-point scale is used. It ranges from 'Very Much' to 'Not Relevant' with 'Very Much' meaning that it negatively affects their daily living and quality of life and 'Not Relevant' meaning that it has no effect on their daily living and quality of life. Baseline
Secondary Central Scalp Alopecia Photographic Scale in African American Women This instrument is a 6-point scale that includes gradations in hair loss from normal (0) to bald scalp (5). Higher numbers denote greater hair loss. Visit 7, Month 12; Visit 9, Month 18-20
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