Skip to content

Effect of omega-3 fatty acid supplementation on diabetes mellitus patients

Effect of omega-3 fatty acid supplementation on homocysteine, lipid profile and insulin resistance in patients with diabetes mellitus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013011312122N1
Enrollment
70
Registered
2013-01-29
Start date
2013-04-09
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

type 2 diabetes. Non-insulin dependent diabetes mellitus

Interventions

Intervention 1: omega-3, 1 gr soft gel, twice a day for 6 weeks. Intervention 2: placebo capsule containing inert Polyethylene glucose, 1 gr soft gel, twice a day for 6 weeks.
Treatment - Drugs
omega-3, 1 gr soft gel, twice a day for 6 weeks
placebo capsule containing inert Polyethylene glucose, 1 gr soft gel, twice a day for 6 weeks

Sponsors

Yazd Shahid Sadoughi University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: patients with diagnosed diabetes and age of 25 to 60 years; a minimum of 5 years experience in diabetes; without any kidney; liver heart; thyroid, bleeding disorders or malignancies; not taking omega-3 supplements in recent months; not using insulin therapy; not pregnant or lactating. exclusion criteria: taking less than 80% of soft gels; changing the type and dose of routine medicine; consume B vitamins supplements during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum homocysteine. Timepoint: baseline and after 6 weeks. Method of measurement: enzymatic cycling using Reagent kit.;Fasting blood glucose. Timepoint: baseline and after 6 weeks. Method of measurement: enzymatic.;Fasting serum insulin. Timepoint: baseline and after 6 weeks. Method of measurement: ELISA assay.;Insulin resistance. Timepoint: baseline and after 6 weeks. Method of measurement: HOMA-IR calculation.;Beta cells function. Timepoint: baseline and after 6 weeks. Method of measurement: HOMA-IR calculation.;Serum Triglycerides. Timepoint: baseline and after 6 weeks. Method of measurement: enzymatic.;Total Cholesterol. Timepoint: baseline and after 6 weeks. Method of measurement: enzymatic.;HDL- Cholesterol. Timepoint: baseline and after 6 weeks. Method of measurement: enzymatic.;LDL-Cholesterol. Timepoint: baseline and after 6 weeks. Method of measurement: Friedewald formula.;Insulin sensitivity. Timepoint: baseline and after 6 weeks. Method of measurement: HOMA-IR calculation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFaezeh Poursoleiman

Yazd Shahid Sadoughi University of Medical Sciences.

f.poursoleiman@ssu.ac.irf_po_yazd@yahoo.com+98 35 1623 4120

Outcome results

None listed

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