CTRI/2022/11/047692
Not yet recruiting
Phase 4
Comparison of therapeutic efficacy and safety of two concentrations of intra-lesional triamcinolone acetonide in patchy alopecia areata of the scalp: an open label randomized trial
I0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: L639- Alopecia areata, unspecified
- Sponsor
- I
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients of both sexes(males and females), aged \>13 years with AA,
- •2\.Patients having AA on the scalp with \<50% involvement.
- •3\.Patients who had not taken any form of treatment in the last 8 weeks.
- •4\.Patients who are willing to sign the written consent form before participating in the study
Exclusion Criteria
- •1\.Patients aged \<13 years
- •2\.Patients with alopecia totalis, alopecia universalis and ophiasis.
- •3\.Patients having skin diseases affecting the scalp.
- •4\.Patients with active infection at the local site and with keloidal tendency.
- •5\.Pregnant or lactating women or immuno\-compromised patients or patients with bleeding or coagulation disorders
Outcomes
Primary Outcomes
Not specified
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