CTRI/2019/01/017202
Completed
Phase 2
Comparative study of the safety and therapeutic efficacy of oral cyclosporine and oral betamethasone minipulse therapy in the treatment of alopecia areata.
Shibashis Chatterjee0 sites60 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: L639- Alopecia areata, unspecified
- Sponsor
- Shibashis Chatterjee
- Enrollment
- 60
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients consenting for the study.
- •2\.All the patients presenting with circumscribed patch of hair loss without any signs of inflammation or scarring,of size \> 3cm in diameter.
- •3\.Patients who have symptoms of 3 months or more duration.
- •4\.Patients who have not taken any other modalities of treatment in the last 3 months.
Exclusion Criteria
- •1\.Patients who are k/c/o hypertension.
- •2\.Patients with secondary infection.
- •3\.Pregnant and lactating females.
- •4\.Patients with pre\-existing renal and liver diseases.
- •5\.Patients with diabetes mellitus.
- •6\.Patients having any Autoimmune disease like SLE, Sjogrenâ??s Syndrome,etc.
- •7\.Patients having contraindications to the drugs used in the study.
Outcomes
Primary Outcomes
Not specified
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