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Enrolling by Invitation

NCT Number: NCT07352618

"Effect of Omega-3 Supplementation as Add on Therapy on Glycemic Control and Lipid Profile in Type2 Diabetes Mellitus."

The goal of this clinical trial is to learn if Omega-3 works to control glycemic status, improve lipid profile in Type2 Diabetic patients. It will also learn about the safety of drug Omega-3. The main questions it aims to answer are:

Does drug Omega-3 control glycemic status, improve lipid profile in Type2 Diabetic patients? What medical problems do participants have when taking drug Omega-3? Researchers will compare Omega-3 to a placebo(a look-alike substance that contains no drug)to see if Omega-3 works to treat Type 2 Diabetic patients.

Participants will take Omega-3 or a placebo twice daily for 12 weeks. Baseline and 12 weeks after FPG, HbA1c,Serum Lipid profile, Omega-3 level will be monitored.

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Key information

Age range

25 year–75 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Bangladesh Medical University

Dhaka, Bangladesh

About this study

Diabetes Mellitus is a common endocrine disorder. T2DM is characterized by polyuria, polydipsia, polyphagia. It affects both men and women. T2DM is strongly associated with impaired insulin sensitivity, insulin resistance, dyslipidaemia, hypertension, and central obesity. Omega-3 polyunsaturated fatty acid has been shown to exert beneficial effect on lipid metabolism and insulin sensitivity.

Aim of the study: We aimed to evaluate the effect of Omega-3 supplementation as add on therapy on glycemic control and lipid profile in Type 2 diabetes mellitus patients.

Methodology: This research will be a single center study, utilizing a double-blind, randomized placebo-controlled trial design. A total of 66 men and women, with diagnosed T2DM, age range from 25-75 years will randomly be assigned to receive either Omega-3 supplementation or placebo for 12 weeks. Biochemical and anthropometric measurements, including Fasting plasma glucose, HbA1c, lipid profile, blood pressure, BMI, waist-hip ratio and waist-to-height ratio will be assessed at baseline and post-treatment. Follow-up assessments will be conducted after supplementation for 12 weeks to evaluate the sustainability of biochemical changes. For independent samples; t-test will be utilized to analyze the average differences in metabolic biomarker levels between the group receiving Omega-3 supplements and the group receiving a placebo. The Chi-square test or Fisher's exact test will be employed to compare the percentage of participants may show a significant change in metabolic biomarker in the group that received Omega-3 versus the group that received a placebo.

Pearson or Spearman correlation tests will be used to explore any relationships between baseline Omega-3 levels and FPG, HbA1c and lipid profile levels, as well as between the change in Omega-3 levels and the change in FPG, HbA1c and lipid profile levels.

Conclusion: Combining Omega-3 supplementation with the conventional treatment could potentially have a substantial impact on lipid profile and glycemic control in patients with T2DM.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age above 25 years up to 75 years
  • Old and newly diagnosed case of Type2 DM.
  • Patient receiving conventional diabetic treatment like OAD or insulin or both
  • Patient may have altered lipid profile or not
  • Both male and female patient
  • Patient's HbA1c level within 8.0%

Exclusion criteria

  • Pregnancy and lactating mother.
  • History of known Type1 diabetes mellitus, secondary diabetes, drug induced diabetes, drugs interfering body weight.
  • Patient with acute illness, liver disease, psychiatric disorder
  • Patients receiving Omega-3 supplementation within the last three months.
  • Known allergy to fish oil or Omega-3 supplements.

Treatment and study plan

Omega-3 fatty acids

Dietary Supplement

Participants received Omega-3 1gm capsule orally twice daily for 12 weeks

Placebo

Dietary Supplement

Participants received Omega-3 placebo capsule twice daily for 12 weeks

Primary outcomes

  1. Changes in lipid profile

    Time frame: 12 weeks

    (triglycerides, HDL-Cholesterol)

  2. Change in Plasma Omega-3 level

    Time frame: 12 weeks

    changes in plasma DHA and EPA conc

  3. Change in HbA1c

    Time frame: 12 weeks

  4. Improvement of Fasting Plasma Glucose

    Time frame: 12 weeks

Secondary outcomes

  1. Change in Blood Pressure (Systolic and Diastolic Blood Pressure)

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

Bangladesh Medical University

Other

Registry information

Official study title

"Effect of Omega-3 Supplementation as Add on Therapy on Glycemic Control and Lipid Profile in Type2 Diabetes Mellitus: A Randomized, Double-Blind, Placebo-Controlled Trial"

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 20, 2026
Registry last updated
Jan 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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