A study of patchy hair loss(alopecia areata) by local examination and using an instrument (dermoscope) and a study of effectiveness of an applicant called Diphenycyprone
Phase 4
- Conditions
- Health Condition 1: L639- Alopecia areata, unspecifiedHealth Condition 2: L639- Alopecia areata, unspecified
- Registration Number
- CTRI/2019/04/018380
- Lead Sponsor
- Yenepoya Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients visiting Yenepoya medical college hospital during the study period with a clinical diagnosis of alopecia areata voluntarily consenting to participate in the study
For the Diphencyprone treatment group: Patients who have failed any one form of treatment for alopecia areata and those willing for regular follow up.
Exclusion Criteria
Patient with immunocompromised status, pregnancy, lactating mothers, severe systemic illnesses
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Determining clinical profile of Alopecia areata <br/ ><br>2. Determining the Dermoscopic featuresTimepoint: 18 months
- Secondary Outcome Measures
Name Time Method Efficacy of Diphencyprone in Alopecia areataTimepoint: 12 WEEKS