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Therapeutic Effect of Pioglitazone in Diabetic Patients with Renal Transplantation

Clinical Trial of Effect of Pioglitazone Therapy on hs-CRP and Lipid Profile in Diabetic Patients with Renal Transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014050117413N2
Enrollment
58
Registered
2014-05-12
Start date
2013-06-10
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

Condition 1: Insulin-dependent diabetes mellitus. Condition 2: Non-insulin-dependent diabetes mellitus. Condition 3: Kidney transplant failure and rejection. Insulin-dependent diabetes mellitus Non-insulin-dependent diabetes mellitus Kidney transplant failure and rejection

Interventions

Intervention 1: Daily one 15 mg Pioglitazone tablet addition to routine insulin therapy for four months. Intervention 2: Daily one placebo tablet addition to routine insulin therapy.
Treatment - Drugs
Placebo
Daily one 15 mg Pioglitazone tablet addition to routine insulin therapy for four months
Daily one placebo tablet addition to routine insulin therapy

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who had undergone kidney transplantation at Labbafinejad hospital within one month after transplantation and diagnosis of diabetes had been confirmed, without age or gender limitation. Exclusion criteria: Cigarette smoker; patients with heart failure FC II & III; hepatitis B and C; GFR less than 30; pregnancy; acute rejection with progressive renal impairment; creatinine more than 1 mg/dl

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fasting blood glucose. Timepoint: Before treatment and after four months treatment. Method of measurement: Laboratory tests.;Blood uric acid. Timepoint: Before treatment and after four months treatment. Method of measurement: Laboratory tests.;Blood hs CRP. Timepoint: Before treatment and after four months treatment. Method of measurement: Laboratory tests.;Blood Triglyceride. Timepoint: Before treatment and after four months treatment. Method of measurement: Laboratory tests.;Blood Cholesterol. Timepoint: Before treatment and after four months treatment. Method of measurement: Laboratory tests.;Low density lipoprotein (LDL). Timepoint: Before treatment and after four months treatment. Method of measurement: Laboratory tests.;High density lipoprotein (HDL). Timepoint: Before treatment and six months after treatment. Method of measurement: Laboratory tests.

Secondary

MeasureTime frame
Weight. Timepoint: Before treatment and after four months treatment. Method of measurement: Kilograms.;Body mass index. Timepoint: Before treatment and after four month treatment. Method of measurement: kg/m2.;Waste circle. Timepoint: Before treatment and after four months treatment. Method of measurement: Centimeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamidreza Karimi Sari

Students’ Research Committee (SRC), Baqiyatallah University of Medical Sciences, Tehran, IR Iran

dr.karimih@yahoo.com+98 21 8126 4354

Outcome results

None listed

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