Actively Recruiting

Phase 4
Age: 18Years - 60Years
FEMALE
NCT04207931

Treatment Results for Patients With Central Centrifugal Cicatricial Alopecia (CCCA): a Multicenter Prospective Study

Led by Wake Forest University Health Sciences · Updated on 2026-03-31

250

Participants Needed

1

Research Sites

461 weeks

Total Duration

On this page

Sponsors

W

Wake Forest University Health Sciences

Lead Sponsor

T

The Skin of Color Society

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Treatment Results for Patients With Central Centrifugal Cicatricial Alopecia (CCCA): a Multicenter Prospective Study

Who Can Participate

Age: 18Years - 60Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • African-American women, ages 18 to 60 years old
  • Clinical diagnosis and biopsy-proven Central Centrifugal Cicatricial Alopecia
  • Central Scalp Alopecia Scale severity between 1 and 4
  • Treated at Wake Forest Baptist Health Dermatology Outpatient Clinic
Not Eligible

You will not qualify if you...

  • Presence of other types of hair loss besides CCCA
  • Other inflammatory scalp diseases except mild seborrheic dermatitis
  • Use of topical treatment for CCCA within the past 4 months
  • Use of long-term oral antibiotics for hair loss within the past year
  • More than two rounds of intralesional steroid injections to the scalp in the past year

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Wake Forest Baptist Health Department of Dermatology

Winston-Salem, North Carolina, United States, 27157

Actively Recruiting

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Research Team

A

Amy J McMichael, MD

CONTACT

J

Judy Holbrook, CRC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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