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A study to compare efficacy of topical 2 percent tofacitinib ointment versus 0.1 percent tacrolimus ointment in patients of vitiligo

Efficacy of 2 percent Tofacitinib ointment versus 0.1 percent Tacrolimus ointment in patients of vitiligo - A hospital based double blinded randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079688
Enrollment
84
Registered
2025-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L80- Vitiligo

Interventions

Intervention1: Tofacitinib: Patients in one group will be applying 1 finger tip unit of Tofacitinib 2 percent ointment topically over vitiligo lesions for a total duration of 24 weeks once daily durin

Sponsors

Dr Kavita Swami
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: vitiligo patients with affected total body surface area less than 5 percent, who are equal to or older than 18 years of age not taking any systemic treatment from past 3 months

Exclusion criteria

Exclusion criteria: vitiligo patients who have only mucosal involvement, or TBSA more than 5 percent, or those requiring systemic treatment, or pregnancy or lactation, or younger than 18 years of age, or having known hypersensitivity to momatasone cream, tacrolimus ointment or tofacitinib ointment not consenting to the study

Design outcomes

Primary

MeasureTime frame
Number and percentage of patients achieving treatment success which is defined by Vitiligo noticebility scale grade more than 3 or more than 50% repigmentation in vitiligo patch in both groups after 24 weeks of treatment. Timepoint: 24 weeks

Secondary

MeasureTime frame
1. Number and percentage of patients achieving treatment success which is Vitiligo noticebility scale grade more than or equal to 3 or more than 50% repigmentation as per various types of vitiligo at the end of 24 weeks. 2. Number and percentage of patients who had any improvement in leukotrichia. 3. Number of patients achieving treatment success which is Vitiligo noticebility scale grade more than or equal to 3 or more than 50% repigmentation in acral and non acral vitiligo in both groups at the end of study.Timepoint: 24 weeks

Countries

India

Contacts

Public ContactDr Kavita Swami

All India Institute of Medical Sciences Gorakhpur

shivangi.rana356@gmail.com8860565443

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026