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Comparison of Betamethasone and Methotrexate efficacy in the Treatment of Alopecia Areata

Phase 3
Conditions
Alopecia Areata.
Alopecia areata
Registration Number
IRCT20181226042136N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
36
Inclusion Criteria

The scalp involvement rate more than 50%
The disease is resistant to systemic and topical combination therapy
The patient is satisfied with the study

Exclusion Criteria

Pregnancy or Breastfeeding
Hb less than 9mg/dl
Leukocyte less than 4000
Platelet less than 100000
Potassium is less than 3.5
Liver enzymes 2 times more than the reference limit
ESR above reference limit
Positive Stool Test for Strongyloides stercoralis
Positive tests for viral hepatitis
Use of any systemic drug a month before the start of the study
There is a contraindication for betamethasone (diabetes, high blood pressure, drug allergy, active infection, recent surgery history, osteoporosis, stomach ulcer and psychosis, or depression)
Sensitivity to methotrexate

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Photographic Scoring for patients with Alopecia Areata. Timepoint: Before the start of the study and 3 , 6, 9 months after the start of treatment. Method of measurement: Photographic Scoring.;Visual Analogue Scale Score in patient with Alopecia Areata. Timepoint: Before the start of the study and 3 , 6, 9 months after the start of treatment. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
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