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efficacy and safety of oral pioglitazone in treatment of lichen planopilaris

efficacy and safety of adding oral pioglitazone to standard treatment in lichen planopilaris

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230415057912N1
Enrollment
30
Registered
2023-12-07
Start date
2023-05-01
Completion date
Unknown
Last updated
2024-01-22

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: Methotrexate group with pioglitazone, test dose of MTX is given in the amount of 15 mg by injection. 1 week later, CBC, liver enzymes and kidney function will be ch

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: a disease that is resistant to treatment. It means that the treatment has been ineffective for at least 6 months. Newly diagnosed patients who have not yet received treatment. Patients who have been treated before and whose disease is still active. Patients who, for any reason, have discontinued any previous medication 1 month before entering the study and have not used any other medication at the time of the study. Patients between 18 and 50 years old

Exclusion criteria

Exclusion criteria: Pregnancy or breastfeeding wbc<3000 platelet<100000 hemoglobin<9 Liver enzymes that are too normal for reference and active liver disease Positive tests for viral hepatitis Heart failure Type 1 diabetes Allergy to pioglitazone and methotrexate Bladder cancer Tissue edema

Design outcomes

Primary

MeasureTime frame
Lichen Planopilaris Activity Index. Timepoint: Months 0, 2, 4, and 6 after starting the drug. Method of measurement: Handyscope dermatoskope (FotoFinder System GmbH, Bad Brinbach, Germany.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFereshteh Sherafat

Esfahan University of Medical Sciences

dr.fereshteh69@yahoo.com+98 910 205 0355

Outcome results

None listed

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