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The effect of nano bandage for vitiligo treatment

Phase 2
Recruiting
Conditions
Vitiligo.
Vitiligo
Registration Number
IRCT20130812014333N98
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

Patients with unstable vitiligo

Exclusion Criteria

Pregnancy and lactation
Other systemic diseases such as cardiovascular disease
Renal or liver failure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The skin lesion size. Timepoint: At the beginning of the study, ten days and six months after the end of the study. Method of measurement: Using the digimizer software.;Change in the color of skin lesions. Timepoint: At the beginning of the study, ten days and six months after the end of the study. Method of measurement: Using the digimizer software.
Secondary Outcome Measures
NameTimeMethod
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