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Clinical Trials/CTRI/2024/02/063353
CTRI/2024/02/063353
Not yet recruiting
Phase 3

To compare the efficacy and adverse effects of oral tofacitinib and oral methylprednisolone mini-pulse and combination of both in treatment of alopecia areata: A Randomized Controlled Trial. - NI

Institute of Medical Sciences BH0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: L639- Alopecia areata, unspecified

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: L639- Alopecia areata, unspecified
Sponsor
Institute of Medical Sciences BH
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Institute of Medical Sciences BH

Eligibility Criteria

Inclusion Criteria

  • •1\. Clinically diagnosed cases of alopecia areata with severity of alopecia tool (SALT) score of 10 % or over.
  • •2\. Age: 18 to 65 years
  • •3\. Patients not taking systemic drug in last 1 month and topical treatment in last 15 days.
  • •\- All participants who give consent for the study

Exclusion Criteria

  • •1\. Patients having history or active tuberculosis.
  • •2\. Patients with Pregnancy and lactating mother.
  • •3\. Patients with uncontrolled renal, hepatic,
  • •hematological or heart disease.
  • •4\. Patients with diabetes mellitus and hypertension.

Outcomes

Primary Outcomes

Not specified

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