CTRI/2024/01/061673Not yet recruitingPhase 4
Comparative study on the therapeutic efficacy of topical bimatoprost (0.03%) ophthalmic solution and tacrolimus (0.1%) ointment in stable vitiligo. - NI
Eras Lucknow Medical College and Hospital0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Stable vitiligo patients involving less than 5 % of body surface area attending the dermatology OPD at Era Lucknow Medical College and Hospital
Exclusion Criteria
- •1. Vitiligo patients who took treatment in last 3 months
- •2. Patient having hypersensitivity to tacrolimus ointment and bimatoprost ophthalmic solution.
- •3. Pregnant and lactating women
Investigators
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