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Effects omega-3 fatty acid supplementation in the treatment of diabetes

Effects of omega-3 fatty acid supplementation on metabolic profiles, hs-CRP and biomarkers of oxidative stress in diabetic nephropaty patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201502255623N36
Enrollment
60
Registered
2015-03-10
Start date
2015-03-11
Completion date
Unknown
Last updated
2019-10-07

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

Interventions

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients with diabetic nephropathy aged 45 to 85 years. Proteinuria level>0.3 g/24 h, with or without elevation of serum creatinine levels

Exclusion criteria

Exclusion criteria: The intake of omega-3 fatty acid supplements within 3 months Patients with uncontrolled diabetes The current use of warfarin Malignancy and/or liver cirrhosis.

Design outcomes

Primary

MeasureTime frame
Insulin resistance. Timepoint: Baseline and End-of-trial. Method of measurement: Calculation using HOMA formula.;Insulin. Timepoint: Baseline and End-of-trial. Method of measurement: ELISA kit.

Secondary

MeasureTime frame
High-sensitivity C-reactive protein. Timepoint: Baseline and End-of-trial. Method of measurement: ELISA test.;Malondialdehyde. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Glutathione. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Total antioxidant capacity. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Nitric oxide. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Triglycerides. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic kit.;Total cholesterol. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic kit.;HDL. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic kit.;Fasting blood sugar. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic kit.;LDL. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic kit.;Blood Urea Nitrogen. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Serum Creatinine. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZatollah Asemi

Kashan University of Medical Sciences

asemi_r@yahoo.com+98 31 5562 0608

Outcome results

None listed

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