Health Condition 1: L639- Alopecia areata, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All consenting patients of alopecia areata with SALT score less than 25% scalp involvement of either gender aged 18 years and above visiting in Dermatology OPD
Exclusion criteria
Exclusion criteria: Patients who have taken any form of treatment in past 3 months Immunocompromised patients or patients on immunosuppressive therapy will be excluded Pregnant or lactating mothers Patient with a history of hypersensitivity to tofacitinib or calcipotriol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess and compare the efficacy of topical tofacitinib cream (2%) and topical calcipotriol ointment (0.005%) in promoting hair regrowth and minimizing disease progression in individuals with alopecia areataTimepoint: 4 weeks,8 weeks,12 weeks, 16 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| To analyse the efficacy of tofacitinib cream (2%) in alopecia areata. To analyse the efficacy of calcipotriol ointment (0.005%) in alopecia areata. To analyse potential side effects & patientâ??s tolerability associated with the use of topical tofacitinib cream (2%) & topical calcipotriol ointment (0.005%).Timepoint: 4 weeks,8weeks,12weeks,16weeks | — |
Countries
India
Contacts
Eraâ??s Lucknow Medical College and Hospital