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

Comparative of Betamethasone pulse, Methotrexate pulse and Betamethasone Combination using Methotrexate pulse Therapy in Treatment of Severe Alopecia Areata

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181226042136N1
Enrollment
36
Registered
2019-01-15
Start date
2017-06-22
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Alopecia Areata. Alopecia areata

Interventions

Intervention 1: Intervention group 1: The first group will be treated with 3 mg betamethasone per oral in the form of 0.5 mg tablets (made by Iran Hormones Co.) and with a dose of 1 mg for breakfast,

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZakiye Ganjei

Esfahan University of Medical Sciences

z.ganjei@gmail.com+98 31 3668 5555

Outcome results

None listed

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