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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02019680
Other study ID # 140034
Secondary ID 14-NR-0034
Status Withdrawn
Phase N/A
First received December 20, 2013
Last updated June 30, 2017
Start date December 10, 2013
Est. completion date May 9, 2017

Study information

Verified date May 9, 2017
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background:

- Heart disease is the leading cause of death in the United States. Eating fruits and vegetables with chemicals called flavonoids may protect against heart disease and improve blood flow to the heart. They are found in blackcurrant berries. Oils found in fish and mussels called omega-3 fats have also been shown to protect the heart. Researchers want to know if blackcurrant extract and omega-3 fats can improve blood flow, which may increase blood to the heart. They also want to learn about the health of blood vessels and how the heart works.

Objective:

- To learn if blackcurrant extract and omega-3 fats will improve blood flow and make the heart beat stronger.

Eligibility:

- Healthy adults 55 to 75 years old.

Design:

- Participants will be screened with medical history, physical exam, and blood tests.

- Visit 1 will take 6 7 hours.

- Participants will have physical exam and blood and urine tests.

- A small device like a microphone will be placed on their arm to take pictures of blood vessels. A blood pressure cuff will be tightened on their arm and more pictures will be taken.

- Blood pressure cuffs will be placed on their arms and legs. They will be tightened at the same time and blood pressure will be measured.

- Participants will answer questions about their eating and exercise.

- Every 8 weeks, participants switch from taking blackcurrant and/or omega-3 tablets to a placebo to no tablets. <TAB>

- Every 8 weeks, they will have another shorter clinic visit that will repeat most of visit 1.


Description:

Numerous studies have shown the beneficial effects of fruits, vegetables and omega-3 fatty acids in reducing the risk of cardiovascular disease. The cardioprotective properties may be attributed to the bioactive compounds found in fruits and vegetables called flavonoids. High concentrations of flavonoids with antioxidant activity are found in blackcurrant extract. Flavonoids like omega-3 fatty acids may improve vascular function by increasing the bioavailability of nitric oxide, a potent vasodilator. PCSO-524 (Pernacanaliculus supercritical oil) is of particular interest as a rich source of omega-3 fatty acids derived from the green-lipped mussel. The objectives of this study are to determine the effects of blackcurrant extract, PCSO-524 or the combination of blackcurrant extract & PCSO-524 on endothelial function (flow-mediated brachial artery dilation) and arterial stiffness (cardioankle vascular index) as indicators of cardiovascular risk and atherosclerosis. These indices also provide an assessment of structure and function of the artery. The effects of the supplements on biomarkers of vascular health (endothelial dysfunction, inflammation, injury, oxidative stress, nitric oxide status), lipids and fatty acid profile, and flavonoid profiles will also be determined. In a randomized, double-blind, placebo-controlled trial, 122 healthy older adults (ages 55-75) will be given either blackcurrant extract (1000 mg), PCSO-524 (400 mg), or blackcurrant extract (1000 mg) & PCSO-524 (400 mg) daily for 8 weeks while consuming their usual diet. The study will include 4 visits at 8 week intervals consisting of treatment, washout and placebo phases.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 9, 2017
Est. primary completion date May 9, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years to 75 Years
Eligibility - INCLUSION CRITERIA

- Men and women between the ages of 55-75 years

- In general good health as determined by screening evaluation

- Normal or pre-hypertensive blood pressure (e.g. Systolic less than or equal to 139 mm Hg and Diastolic less than or equal to 89 mm Hg

- Normal or mild hyperlipidemia (e. g. Total Cholesterol less than or equal to 239, LDL less than or equal to 159, Triglycerides less than or equal to 199, HDL less than or equal to 40 mg/dL)

- BMI between 18.5 to 25 kg/m^2

- Willingness and ability to give consent

- Willingness to make time commitment for the study

EXCLUSION CRITERIA

- Progressive or unstable disease of any body system including cardiovascular, pulmonary, gastrointestinal, central nervous system, psychiatric, endocrine, hematologic, renal or immunologic disorders

- Known acute or chronic inflammatory disease ( e.g. rheumatoid arthritis, systemic lupus erythematosus, hepatitis)

- Elevated C-reactive protein (CRP) level > 3.0 mg/L

- Elevated fasting blood glucose level > 120 mg/dL

- Elevated lipid profile : Total cholesterol > 239 mg/dL, Triglycerides > 200 mg/dL, LDL >160mg/dL

- Abnormal complete blood count (CBC): White Blood Cell Count < 4 or > 10 K/uL, Red Blood Cell Count < 4 or > 7 M/uL, Hemoglobin < 13 or > 18 g/dL, Hematocrit < 39 or > 52%

- Recent or ongoing alcohol or drug abuse (Subjects with moderate alcohol consumption described as 12oz. of beer, 5oz. glasses of wine, or 1.5 glasses of hard liquor/day or greater alcohol consumption will be excluded.)

- Known sensitivity or allergy to fish oil, or shell fish

- Smoking any tobacco products (cigarettes, pipe, etc.)

- Subjects currently taking fish oil supplements (participation is possible after 2 month washout period)

- Subjects taking blood thinners (i.e., Coumadin, warfarin etc.)

- Subjects with bleeding disorders (i.e., hemophilia)

- Subjects taking cholesterol-lowering, anti-hypertensive, thyroid or hormonal medications

- Subjects taking aspirin, non-steroidal anti-inflammatory (NSAIDS) medications or fish oil on a regular basis unless they were discontinued 14 days prior to their first visit.

- Subjects starting cholesterol-lowering, anti-hypertensive, thyroid or hormonal medications or fish oil during the study

- Subjects taking supplements unless they were discontinued 14 days prior to their first visit.

Study Design


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
National Institute of Nursing Research (NINR) Tufts University

References & Publications (3)

Hertog MG, Feskens EJ, Hollman PC, Katan MB, Kromhout D. Dietary antioxidant flavonoids and risk of coronary heart disease: the Zutphen Elderly Study. Lancet. 1993 Oct 23;342(8878):1007-11. — View Citation

Joshipura KJ, Hu FB, Manson JE, Stampfer MJ, Rimm EB, Speizer FE, Colditz G, Ascherio A, Rosner B, Spiegelman D, Willett WC. The effect of fruit and vegetable intake on risk for coronary heart disease. Ann Intern Med. 2001 Jun 19;134(12):1106-14. — View Citation

Ness AR, Powles JW. Fruit and vegetables, and cardiovascular disease: a review. Int J Epidemiol. 1997 Feb;26(1):1-13. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Endothelial function (flow-mediated brachial artery dilation) and arterial stiffness (cardio-ankle vascular index) 8 weeks x 4
Secondary Biomarkers of vascular health (endothelial dysfunction, inflammation, injury, oxidative stress, nitric oxide status), lipids and fatty acid profile, and flavonoid profiles 8 weeks x 4
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