Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 12:43 AM
Ignite Modification Date: 2025-12-25 @ 12:43 AM
NCT ID: NCT01712867
Eligibility Criteria: Inclusion Criteria: 1. Male or female, age \> 18 years 2. Triglycerides ≥ 200 mg/dL and \< 500 mg/dL 3. Ability to give written informed consent Exclusion Criteria: 1. Female patient who are pregnant or breastfeeding or planning to become pregnant 2. Fasting plasma glucose (FPG) levels \> 110 mg/dL 3. Type 2 diabetes mellitus that is poorly controlled (glycosylated hemoglobin \[HbAlc \] \>8.0% 4. Patients who are under use of lipid altering drugs excluding use of Simvastatin, Atorvastatin, and Rosovastatin for 6 weeks or more 5. Patients who are under use of products containing omega-3 fatty acids or other dietary supplements with potential lipid altering effects 6. History of bariatric surgery or currently on weight loss drugs. 7. Uncontrolled hypertension (BP\>140/90) 8. Subjects with secondary causes of hypertriglyceridemia: alcoholism, dysglobulinemia, thyroid disease that is poorly controlled (TSH\<0.35 or TSH\>5.5) 9. Subjects with an abnormal level of liver enzymes (twice the normal level) 10. Suffered from ischemic event such as myocardial infarction, cerebrovascular accident and angina pectoris in the last 6 months 11. Uncontrolled endocrine or metabolic disease known to influence serum lipids or lipoproteins such as cushing syndrome 12. Gastrointestinal disease that may influence lipid metabolism such as celiac, crohn, colitis or other malabsorption problem 13. Subjects who have had any malignancy. Subjects who have had basal cell carcinoma that have been disease free for at least 3 years are eligible for the study. 14. Consumption of one fish serving (200 grams) or sea food x2 a week or more. 15. HIV infection by history 16. History of hypersensitivity or allergy to fish, fish oil or soy 17. BMI≥35 18. Weight change \> 3 kg during the run-in period 19. Any other reason that, in the opinion of the investigator, prevents the subject from participating in the study or compromise the patient
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT01712867
Study Brief:
Protocol Section: NCT01712867