Status:
UNKNOWN
HDL Function Dietary Supplement Safety and QOL
Lead Sponsor:
Metagenics, Inc.
Collaborating Sponsors:
Hypertension Institute, Nashville
Conditions:
HDL
Health, Subjective
Eligibility:
All Genders
18-85 years
Phase:
NA
Brief Summary
Nutritional supplements are routinely purchased by consumers with suboptimal HDL to support their health, lifestyle and overall quality of life. Many such products receive minimal evaluation prior to ...
Detailed Description
High density lipoprotein cholesterol (HDL), often considered the 'good cholesterol,' plays an essential role in reverse cholesterol transport (RCT), and has anti-inflammatory, anti-oxidative, and anti...
Eligibility Criteria
Inclusion
- Men: Total HDL of equal to or less than 38 mg / dL in men AND a low HDL-P of less than or equal to 7200 by Spectracell LPP Plus.
- Women: Total HDL equal to or less than 45 mg/dl in women, AND a low HDL-P of less than or equal to 7200 by Spectracell LPP Plus.
- Willingness to maintain current lifestyle (diet and exercise) practices
- Willingness to eat fish no more than twice per week and keep intake stable throughout the study
- Willingness to give written informed consent to participate in the study
- Willingness to follow lifestyle instructions for 24 hours prior to the study visit.
- No known food allergy or intolerance to the ingredients in the study product (fish, shellfish)
- Not currently taking (washout of at least 30 days required) any other supplements that would interfere with the study results
- Not currently taking (washout of at least 30 days required) any other supplements designed to support HDL.
Exclusion
- Use of medications classified as narcotics 30 days prior to Screening and for the duration of the study.
- Use of an investigational drug or participation in an investigational study within 30 days prior to Day 1 and for the duration of the study.
- Current use (at least 30 days wash-out required) of any lipid lowering medication which, in the view of the PI, may interfere with the results.
- Known allergy or hypersensitivity to study product.
- No initiation of a new or change of an existing exercise regimen within 15 days prior to Day 1 and for the duration of the study.
- No initiation of a new or change of an existing food plan 30 days prior to Day 1 and for the duration of the study.
- No current involvement or within 30 days of Day 1 of a significant diet or weight loss program such as Atkin's or other Low-Carb diet programs, very low calorie liquid diet programs (such as Optifast, Medifast and/or HMR) or any diet that has led to a weight loss of 5% of body weight over a period of 10 weeks.
- No serious, unstable illnesses including cardiovascular, hepatic, renal, gastrointestinal, respiratory, endocrine, neurologic, immunologic, or hematologic disease.
- Known infection with Human Immunodeficiency Virus (HIV), Tuberculosis or Hepatitis B or C.
- Subjects with a current diagnosis or personal history of:
- Previous myocardial infarction within 5 years, Unstable angina, Previous stroke or transient ischemic attack (TIA) within 5 years, Uncompensated congestive heart failure, Previous percutaneous transluminal coronary angioplasty (PCTA) or stent within 5 years, Previous coronary artery bypass grafts (CABG) within 5 years
- Type 1 diabetes mellitus
- Any significant liver or kidney disease such as cirrhosis or non-alcoholic fatty liver disease, glomerulonephritis, and/or undergoing dialysis treatment. Cr over 2.5 mg/dL.
- Any malignancy (with the exception of basal or squamous cell carcinoma of the skin if adequately treated and no recurrence for \>5 years).
- Any serious mental illness including depression, manic episodes, post-traumatic disorder, obsessive-compulsive disorder, personality disorders, history of attempted suicide or violence within 12 months prior to Screening and for the duration of the study.
- Any personal history of bipolar disorders, schizophrenia or psychotic behaviors.
- Personal history of seizure disorder other than a single childhood febrile seizure that fully resolved.
- Known presence of raised intraocular pressure or history of narrow angle glaucoma.
- A major medical or surgical event requiring hospitalization within the preceding 3 months
- The presence of any disease which influences digestion and absorption of nutrients
- History of any bariatric surgery procedure
- Consumption of alcohol the evening prior to any study visit
- Use of drugs of abuse (such as marijuana, cocaine, phencyclidine \[PCP\] and methamphetamine) within 12 months prior to Screening and for the duration of the study.
- History of alcohol abuse or a diagnosis of alcoholism within 12 months prior to Screening and for the duration of the study.
- Inability to comply with study and/or follow-up visits.
- Any other concurrent condition which, in the opinion of the Investigator, would preclude participation in this study or interfere with compliance.
- Pregnancy
- Females of child bearing age not on an accepted contraception control method
Key Trial Info
Start Date :
September 18 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 30 2022
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT04097119
Start Date
September 18 2019
End Date
December 30 2022
Last Update
April 6 2022
Active Locations (1)
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1
Hypertension Institute
Nashville, Tennessee, United States, 37205