Skip to content

The effect of Docosahexaenoic acid on factors influencing vascular thickness and function in diabetic patients

The effect of DHA supplementation on factors influencing vascular thickness and intima-media smooth muscle proliferation in patients with type 2 diabetes mellitus

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013071213964N1
Enrollment
72
Registered
2013-09-15
Start date
2013-09-06
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: Type 2 Diabetes melitus. Condition 2: Atherosclerosis. non-insulin-dependent diabetes Arterial sclerosis

Interventions

Intervention 1: Intervention group: DHA supplement (2 gr per day , 3 month). Intervention 2: Control group: Placebo capsule (containing Sunflower oil similar to DHA capsule) with similar dose (2 gr p
Treatment - Drugs
Placebo
Control group: Placebo capsule (containing Sunflower oil similar to DHA capsule) with similar dose (2 gr per day) and similar period (3 month)
Intervention group: DHA supplement (2 gr per day , 3 month)

Sponsors

Tehran University of Medical Sciences
Lead Sponsor
Endocrinology and Metabolism Research Institute
Collaborator

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Type 2 diabetic patients (both males and females); 30-70 years old age; BMI range between 18.5 to 35 kg/m2 Exclusion criteria: Insulin therapy; any type of Cancer; Liver, Kidney, Coagulation and Thyroid disorders; Cardiovascular diseases such as Angina Pectoris, Myocardial infarction, Stroke; consumption of Anticoagulants, ant-inflammatory and lipid lowering agents such as Fibrates; Thiazolidinedione’s therapy; History of Allergic reaction to fish or fish oil; Daily consumption of fish or fish oil supplements; Supplementation with vitamin A,D and B6; Pregnancy and Lactating; lack of usage more than 10% of administered tablets.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Interleukin 6 gene expression. Timepoint: start and end of intervention. Method of measurement: Real time PCR.;TNF-a gene expression. Timepoint: start and end of intervention. Method of measurement: Real time PCR.;ADMA. Timepoint: start and end of intervention. Method of measurement: ELISA.;SCD163. Timepoint: start and end of intervention. Method of measurement: ELISA.;Telomerase activity. Timepoint: start and end of intervention. Method of measurement: PCR-ELISA kit.;Total cholesterol. Timepoint: start and end of intervention. Method of measurement: Turbidimeter.;Triglyceride. Timepoint: start and end of intervention. Method of measurement: Turbidimeter.;HDL- cholesterol. Timepoint: start and end of intervention. Method of measurement: Turbidimeter.;LDL-cholesterol. Timepoint: start and end of intervention. Method of measurement: Friedewald formula.;Fasting Blood Sugar. Timepoint: start and end of intervention. Method of measurement: Turbidimeter.;Fasting insulin. Timepoint: start and end of intervention. Method of measurement: ELISA.;Insulin resistance. Timepoint: start and end of intervention. Method of measurement: Formula.;Glycated hemoglobin. Timepoint: start and end of intervention. Method of measurement: Kit.

Secondary

MeasureTime frame
Vascular function and proliferation of smooth muscle cells in intima media. Timepoint: start and end of intervention. Method of measurement: Studding the effective factors in vascular function and proliferation of smooth muscle cells in intima media and also comparison of these factors in two intervention and control groups.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactOmid Toupchian

Tehran University of Medical Sciences

o-toupchian@tums.ac.ir+98 21 8862 2706

Outcome results

None listed

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