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Assessing the effectiveness of Methotrexat versus Azathioprine on disease activity index in Lichen planopilaris patients

Comparing the effectiveness of Methotrexate versus Azathioprine on disease activity index in Lichen planopilaris patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191006045005N2
Enrollment
32
Registered
2021-03-29
Start date
2021-04-21
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Lichen planopilaris. Lichen planopilaris

Interventions

Intervention 1: Intervention group 1: 16 patients, Methotrexate oral tablet (anti-neoplastic) made by Zahravi Pharmaceutical Co. 15 mg/week for 6 month. Intervention 2: Intervention group 2: 16 patien

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with local disease that does not respond to topical treatment after one month Patients with extensive scalp involvement as the first line treatment. Patients should have discontinued any previous systemic medication 1 month prior to admission to the study. Ages 18-65

Exclusion criteria

Exclusion criteria: Pregnancy or lactation Leukocytes less than 3000 (leukopenia of any etiology) Platelets less than 100000 Hemoglobin less than 9 Liver enzymes more than 2 time the reference limit Positive for viral hepatitis tests Consumption of Allopurinol

Design outcomes

Primary

MeasureTime frame
Lichen planopilaris Activity Index. Timepoint: Measurement of Lichen planopilaris Activity Index at the beginning of the study (prior to treatment) and 2, 4, and 6 months after the treatment. Method of measurement: Using an oral questionnaire and clinical examination of patient for items in lichen planopilaris activity index.;Photography. Timepoint: Photography at the beginning of the study(prior to treatment) and 2,4 and 6 month after treatment. Method of measurement: Professional camera for dermatologist.;Dermoscopy. Timepoint: Dermoscopy at the beginning of the study(prior to treatment) and 2,4 and 6 month after treatment. Method of measurement: Handyscope fotofinder system.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Hajheidari

Esfahan University of Medical Sciences

parisahajheidarii@resident.mui.ac.ir0098 31 2365742

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026