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The effect of pioglitason on rheumatoid arthritis disease

The effect of pioglitason on disease activity and inflammatory markers of rheumatoid arthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015111425031N1
Enrollment
100
Registered
2016-01-24
Start date
2014-07-02
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

Rheumatoid arthritis. Seropositive rheumatoid arthritis

Interventions

Intervention 1: For twelve weeks, patients treated with Pioglitazone pills, daily 30 mg in intervention group. Intervention 2: For twelve weeks use Pioglitazone pills that filled with starch as placeb
Treatment - Drugs
Placebo
For twelve weeks, patients treated with Pioglitazone pills, daily 30 mg in intervention group
For twelve weeks use Pioglitazone pills that filled with starch as placebo in control group

Sponsors

Vice Chancellor for research of Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 20-65 years old; patients with rheumatoid arthritis (ACR) criteria; disease activity based on DAS-28> 3.2; signed informed consent. Exclusion criteria: comorbidities such as diabetes mellitus, kidney and liver diseases, etc; severe obesity (BMI> 35); uncontrolled hypertension; congestive heart failure (CHF); side effects of pioglitazone drug; acute and active infectious disease; hyperlipidemia TG> 200, total cholestal> 220; indicated to biological drugs.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Disease Activity Score (DAS-28). Timepoint: before and twelve weeks after intervention. Method of measurement: by means of DAS-28 validated questionnaire.;The number of painful and swollen joints. Timepoint: before and twelve weeks after intervention. Method of measurement: visual scale.;Tests (ESR-hs CRP-Cholesterol-HDL-TG-BUN-Cr-AST-ALT-ALK-P). Timepoint: before and twelve weeks after intervention. Method of measurement: Laboratory Kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Talaat Shahmoradi

Arak University of Medical Sciences

t.shamoradi@arakmu.ac.ir+98 86 3366 0666

Outcome results

None listed

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