Differential Thrombogenesis Effects of Eicosapentaenoic Acid (EPA) and Docosahexaenoic Acid (DHA) Mediated by High-Density Lipoprotein (HDL)

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

The goal of this study is to learn more about omega-3 polyunsaturated fatty acids supplementation on blood lipid profile and platelets in patients with high cholesterol levels. The purpose of this research is to gather information on the safety and effect of two different fish oils, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). Participants will: Visit the clinic 3 times during study checkups, tests and blood collection. Randomized to either the EPA or the DHA supplementation group. Be given a 28-day food and activity log.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 69
Healthy Volunteers: f
View:

• Fasting TG levels ≥ 150 mg/dL and \< 500 mg/dL and HDL-C ≤ 40 (men) or ≤ 50 (women)

• LDL-C \> 40 mg/dL and ≤ 130 mg/dL

• Able to provide informed consent and adhere to study schedules

• Agree to follow and maintain a relatively stable and low fatty fish intake diet (\<3 servings per week)

Locations
United States
Rhode Island
Brown University Health - Lipid Clinic
RECRUITING
Providence
Contact Information
Primary
Wenliang Song, MD
WSong@Lifespan.org
4014449851
Backup
Daria Salamevich
DSalamevich@Lifespan.org
4014449857
Time Frame
Start Date: 2025-07-10
Estimated Completion Date: 2028-03-31
Participants
Target number of participants: 80
Treatments
Experimental: DHA group
Participants will receive DHA supplement. 3 gelcaps, three times per day with meals (breakfast, lunch, and dinner). DHA supplement regimen contains 450 mg DHA and minimal EPA (60 mg) per pill.~Participants will be given 28-day food and activity log.
Experimental: EPA group
Participants will receive EPA supplement. 2 gelcaps, two times per day with meals (breakfast and dinner). 1 gelcap consists of 1 gram of EPA.~Participants will be given 28-day food and activity log.
Sponsors
Leads: The Miriam Hospital
Collaborators: National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)

This content was sourced from clinicaltrials.gov

Similar Clinical Trials