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Effects of atorvastatin on diabetic nephropathy

Effects of atorvastatin on proteinuria of type 2 diabetic nephropathy in patients with history of gestational diabetes mellitus

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016100918946N4
Enrollment
42
Registered
2016-11-30
Start date
2014-10-01
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

Diabetic nephropathy. Insulin-dependent diabetes mellitus with renal complications

Interventions

Intervention 1: Intervention group: Atorvastatin 10 mg per day will be administered to the patients in intervention group for 90 days. At the end of the third month, patients will be asked not to use
Treatment - Drugs
Placebo
Intervention group: Atorvastatin 10 mg per day will be administered to the patients in intervention group for 90 days. At the end of the third month, patients will be asked not to use Atorvastatin for
Control group: Daily Placebo will be administered to the patients in control group for 90 days. At the end of the third month, patients will be asked not to use placebo for a month.

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients between 20 to 65 years old; patients with type 2 diabetes mellitus; history of gestational diabetes mellitus; proteinuria levels lower than 3 g/d (nephrotic range); estimated glomerular filtration rate more than 30 mL/min/1.73m2 Exclusion criteria: use of fibrates, statins antagonists, aspirin, allopurinol, ß-blockers, pentoxifylline, fish oil, other antioxidant drugs consumption in past 6 months; active smoking; active coronary artery disease in the previous 6 months; diabetic foot; hepatitis; poorly controlled diabetes (Hb-A1c more than 7.5%)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lipid profile. Timepoint: Before intervention, 90 days after intervention initiation. Method of measurement: Blood samlple.;Serum creatinine. Timepoint: Before intervention, 90 days after intervention initiation. Method of measurement: Blood samlple.;Serum uric acid. Timepoint: Before intervention, 90 days after intervention initiation. Method of measurement: Blood samlple.;Urine Protein. Timepoint: Before intervention, 90 days after intervention initiation. Method of measurement: Blood samlple.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Parviz Saleh

Emam Reza educational-medical center

p.zzss@yahoo.com+98 41 3334 1317

Outcome results

None listed

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