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Comparison of the effects of atorvastatin and rosuvastatin in patients with type 2 diabetes

Comparison of the effects of atorvastatin and rosuvastatin on the levels of furin, blood sugar and lipid indices in patients with type 2 diabetes

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250320065133N1
Enrollment
60
Registered
2025-04-27
Start date
2025-04-21
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Type 2 diabetes. Diabetes mellitus due to underlying condition

Interventions

Intervention 1: First intervention group: Patients with type 2 diabetes mellitus will be treated with atorvastatin to reduce cholesterol and LDL-C and thereby inhibit microvascular and macrovascular c

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 69 Years

Inclusion criteria

Inclusion criteria: Atorvastatin 40 mg per day and rosuvastatin 20 mg per day are recommended for type 2 diabetic patients who require treatment with this drug. Type 2 diabetic patients should not have used statin drugs before treatment. Type 2 diabetic patients aged 19-69 years and healthy individuals aged 19-69 years. Healthy people visit the laboratory for routine examinations or checkups. Healthy individuals without any specific disease, no history of surgery, with normal lipid and sugar profiles Diabetic patients must have had diabetes for at least 2 years. Not receiving insulin

Exclusion criteria

Exclusion criteria: Women who are pregnant or breastfeeding. People who have an active infection or are infected with hepatitis B, hepatitis C, HIV, or tuberculosis. History of any type of cancer Heart attack within the past 6 months or peripheral coronary artery disease Being treated for a chronic condition that requires steroids, such as prednisone. Smoking and alcohol use Women who take contraceptives. Chronic indigestion and diarrhea, failure of important organs, such as the liver, lungs, kidneys, and brain, as well as anemia and diabetic nephropathy.

Design outcomes

Primary

MeasureTime frame
Blood level of furin. Timepoint: Measuring blood levels of furin before treatment with atorvastatin and rosuvastatin and three months after treatment with them. Method of measurement: ELISA method using ELISA reader.;Blood sugar levels. Timepoint: Measurement of blood sugar indicators before treatment with atorvastatin and rosuvastatin and three months after treatment with them. Method of measurement: Photometric method using an autoanalyzer.;Blood lipid index levels. Timepoint: Measurement of blood lipid indices before treatment with atorvastatin and rosuvastatin and three months after treatment with them. Method of measurement: Photometric method using an autoanalyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Nosrati Andevari

Kerman University of Medical Sciences

nosrati.ali70@gmail.com+98 11 4425 3555

Outcome results

None listed

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