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The effect of pioglitazone in psoriasis

The efficacy of methotrexate plus pioglitazone in comparison with methotrexate alone in the management of patients with psoriasis vulgaris: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202279149N1
Enrollment
40
Registered
2012-05-26
Start date
2012-05-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

psoriasis. Plaque psoriasis

Interventions

Intervention 1: oral methotrexate 7.5 t0 15 mg per week for intervention group for 16 weeks, pioglitazone 30 mg per day orally for 16 weeks. Intervention 2: oral methotrexate 7.5 t0 15 mg per week fo
Treatment - Drugs
oral methotrexate 7.5 t0 15 mg per week for intervention group for 16 weeks, pioglitazone 30 mg per day orally for 16 weeks.
oral methotrexate 7.5 t0 15 mg per week for control group for 16 weeks.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: plaque type psoriasis; Indication for systemic therapy; Phototherapy contraindicated; No systemic therapy or phototherapy in last 6 months Exclusion criteria: congestive heart failure; renal disease ; hepatic or pulmonary disease; abnormal hepatic enzymes; diabetes; pregnancy or lactation; potential for childbearing; any other major systemic diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Psoriasis area and severity index (PASI). Timepoint: at weeks 0, 6, 10, 16. Method of measurement: PASI meter.;Dermatology life quality index (DLQI). Timepoint: at weeks 0,6,10,16. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Hepatic enzymes. Timepoint: at weeks 0, 1,2,4,6,10,16. Method of measurement: blood biochemistry.;Complete blood cells (CBC). Timepoint: at weeks 0,1,2,4,6,10,16. Method of measurement: automated analyzer (Automated blood count).;Lipid profile. Timepoint: at weeks, 0, 6,10, 16. Method of measurement: Lipid Blood Tests.;Bun and creatinine. Timepoint: at weeks 0,6,10,16. Method of measurement: blood biochemistry.;Urine analysis. Timepoint: at weeks 0,6,10,16. Method of measurement: Urine test strip.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoroush Daklan

Tehran University of Medical Sciences

daklan@razi.tums.ac.ir soroush.daklan@gmail.com+98 21 5560 9951

Outcome results

None listed

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