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COMPLETED

NCT05015348

Effect of Omega-3 Supplementation on Fasting Triglycerides During Lifestyle Intervention in Adults With Mild-to-moderate Hypertriglyceridemia

Sponsor: Peking Union Medical College Hospital

View on ClinicalTrials.gov

Summary

Patients with hyperlipidemia will be allocated to the intervention or control group randomly. Participants of the intervention group will be provided with Omega-3 PUFA, while participants of the control group will be provided with a placebo which looked same as the drug in the intervention group. During the study, all participants can have nutritional counseling and education for a healthy diet, such as energy restriction when appropriate, reduced saturated fat and refined carbohydrate intake, increased vegetables, whole grains, and dietary fiber, and avoidance of excessive alcohol intake. The lipids, inflammatory factors, weight, and body composition will be assessed and recorded before, at 6 weeks, and at 12 weeks of the study.

Official title: Effect of Omega-3 Supplementation on Fasting Triglycerides During Lifestyle Intervention in Adults With Mild-to-moderate Hypertriglyceridemia: a Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 79 Years

Study Type

INTERVENTIONAL

Enrollment

127

Start Date

2021-12-01

Completion Date

2024-12-01

Last Updated

2026-07-29

Healthy Volunteers

Conditions

Hyperlipidemias

Interventions

DIETARY_SUPPLEMENT

Omega-3 PUFA supplementation

1.788 g/day EPA and 0.630 g/day DHA per day.

OTHER

placebo

the same amont of corn oil as placebo

Inclusion Criteria: * \[1\] Gender and age: male or female, 18 years old and above. * \[2\] Patients were diagnosed with hyperlipidemia. According to the definition of the 2016 guidelines for the prevention and treatment of dyslipidemia in Chinese adults, it meets the clinical diagnostic criteria of mild-moderate hyperlipidemia: hypertriglyceridemia \[TG 1.7-5.4mmol/L\]; Or mixed with TC≥5.2mmol/L\]; Or mixed with LDL-C≥3.4mmol/L\]. * \[3\] Before the study, the subjects fully understood and voluntarily signed the informed consent form, and fully understood the research content, process, and possible adverse reactions. * \[4\] Those who can eat orally. * \[5\] Be able to complete the research according to the requirements of the research protocol and obey the arrangements of doctors and researchers. Exclusion Criteria: * \[1\] Those who are receiving lipid-lowering drugs. * \[2\] Hyperlipidemia caused by secondary causes, such as nephrotic syndrome, hypothyroidism, renal failure, liver disease, systemic lupus erythematosus, glycogen accumulation, myeloma, fat atrophy, acute porphyria, polycystic ovary syndrome, etc; Use diuretics, non-cardiac selective β-receptor blockers, and glucocorticoids, which may cause secondary dyslipidemia. * \[3\] Patients with severe internal and external diseases, such as heart, liver, and kidney dysfunction, acute myocardial infarction, stroke, intracerebral hemorrhage, acute attack of COPD, respiratory failure, etc., in recent 3 months, patients who have undergone surgery in the past 3 months, or any person who is not suitable to participate in this study after clinician evaluation. * \[4\] Have hemorrhagic disease or bleeding tendency. * \[5\] Those who have a history of allergy to omega-3 polyenoic acid preparation. * \[6\] Pregnant and lactating women. * \[7\] Poor compliance, unable to follow up on time or unable to complete the follow-up of medication. * \[8\] In the course of diagnosis and treatment, if there is any seriously abnormal metabolism or further intervention is needed, or the patient is no longer suitable for continuing the study through the assessment of the competent physician, he can withdraw from the study.

Locations (1)

Peking Union Medical College Hospita

Beijing, Beijing Municipality, China