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Study of efficacy and side effects of Pioglitazone in the treatment of psoriasis

Study of efficacy and side effects of Pioglitazone in the treatment of plaque psoriasis vulgaris

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138903013862N2
Enrollment
26
Registered
2010-06-08
Start date
2007-09-26
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. Psoriasis vulgaris

Interventions

oral Pioglitazone 30 mg daily for 12 weeks.
Treatment - Drugs
oral Pioglitazone 30 mg daily for 12 weeks

Sponsors

Research Council of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: new cases of plaque psoriasis which don’t received systematic treatment during last 3 months and for topical treatment last month, patients complete consent form and participate to study consciously. Exclusion criteria: patients who want to leave study deliberately, sensitive to pioglitazone or the same preparations, type one diabetes mellitus, pregnant or lactating women, below 18 years old, with severe hepatic problems (hepatitis, alcoholic or non alcoholic steatohepatitis, cirrhosis), severe cardiovascular disorders (NYHA CLASS III & IV), patients prevent pregnancy only by oral contraceptives, patients that have any of these following side effects during therapy: upper respiratory tract infections and sinusitis, edema and any indicative sign of heart failure, unwanted pregnancy, weight gain, anemia, leuckopenia, hematuria, jaundice and 3 times increment of hepatic enzymes (ALT), any symptom which make patients to leave the study. Patients who used any of these drugs (Oral contraceptives, Gatifloxacin ,Insulin ,sulfunamides ,sulfunylureas, Thioridazine , Gemfibrozil).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Psoriasis severity. Timepoint: monthly untill the end of 12 weeks. Method of measurement: PASI standard method.

Secondary

MeasureTime frame
Side effect. Timepoint: monthly untill end of 12 weeks. Method of measurement: Standard evaluation method for this disease.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadis Yousefzadeh

Research center for skin disease and cutaneous leishmaniasis

hadis_yousefzadeh@yaoo.com+98 51 1732 7027

Outcome results

None listed

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