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To compare the effect of tacrolimus and pimecrolimus in white patch patients

Phase 4
Conditions
Health Condition 1: null- Vitiligo
Registration Number
CTRI/2014/08/004882
Lead Sponsor
TANVI SINGH BHADORIA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Less than 20 % body surface area involvement in patients with vitiligo

Patients having vitiligo not on any other treatment for last 4 weeks

Exclusion Criteria

Involvement of more than 20% body surface area in patients with vitiligo

Immunocompromised patients

History of skin cancers or lymph proliferative disorders

Pregnant or lactating women

Patients on any other treatment for last 4 weeks

Netherton syndrome

Drop outs from the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the efficacy of topical tacrolimus 0.1% ointment and pimecrolimus 1% <br/ ><br> <br/ ><br>cream in vitiligo patientsTimepoint: To compare the efficacy of topical tacrolimus 0.1% ointment and pimecrolimus 1% <br/ ><br> <br/ ><br>cream in vitiligo patients
Secondary Outcome Measures
NameTimeMethod
To compare the safety of Tacrolimus 0.1% ointment and Pimecrolimus 1 %cream in vitiligoTimepoint: 6 months
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