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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01413646
Other study ID # 2009-15
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2010
Est. completion date December 2010

Study information

Verified date July 2019
Source Griffin Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the effects of walnut consumption on endothelial function and lipid markers in overweight patients with at least one factor of metabolic syndrome as compared to the control group.


Description:

The prevalence of obesity in both adults and children in the United States has increased significantly over the past 50 years. More than 66% of adults in the US are now overweight or obese and at least 17% of children in the population at large are now considered overweight.Obesity may be a factor predisposing patients to a myriad of comorbidities that increase the associated mortality rate.Several large prospective trials have documented that obesity is an independent risk factor for mortality from cardiovascular disease (CVD). Considering the major metabolic and biochemical changes that occur in obesity, such as atherogenic dyslipidemia, insulin resistance and hyperinsulinemia, endothelial dysfunction, and chronic inflammatory and prothrombotic states, obesity plays a role in the pathogenesis of systemic atherosclerosis and its clinical complications.

Walnuts are rich in alpha-linolenic acid, an essential omega-3 fatty acid, L-arginine and antioxidants. Polyunsaturated fatty acids and antioxidants have anti-oxidative effects and are thought to help preserve the endothelium's capacity to generate nitric oxide (NO), which acts to promote vasodilation, stabilize platelets, and promote the anti-inflammatory abilities of the endothelium. Evidence of this anticipated effect would have implications for strategies to prevent or retard type 2 diabetes mellitus and cardiovascular disease. Endothelial function testing using high frequency ultrasound imaging of the brachial artery to assess endothelium-dependent flow-mediated dilatation (FMD) offers a non-invasive, uniquely valuable means of assessing aggregated influences on cardiac risk by gauging a physiologic response of the vascular endothelium. Proposed, therefore, is a randomized, controlled, cross-over clinical trial, to assess the effects of walnuts on endothelial function in overweight adults with elevated waist circumference and at least one risk factor of metabolic syndrome.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 2010
Est. primary completion date October 2010
Accepts healthy volunteers No
Gender All
Age group 25 Years to 75 Years
Eligibility Inclusion Criteria:

- Male and female age 25-75 years

- Non-smoker

- Overweight (BMI = 25) with central adiposity as indicated by waist circumference (102 cm. in men / 88 cm. in women)

- Meet one risk factor of the metabolic syndrome.

- blood pressure > 130/85 or taking antihypertensive medication

- fasting plasma glucose (FPG) >100 mg/dL (6.1 mmol/L)

- fasting serum triglycerides level (TG) > 150 mg/dL (1.69 mmol/L)

- fasting high-density lipoprotein (HDL) cholesterol < 40 mg/dL (1.04 mmol/L)in men, and < 50 mg/dL (1.29 mmol/L) in women.

Exclusion Criteria:

- Anticipated inability to complete or comply with study protocol

- Use of lipid-lowering or antihypertensive medications or aspirin unless stable on medication for at least 3 months and willing to refrain from taking medication for 12 hours prior to EF scanning

- Preexisting cardiovascular disease (including symptomatic coronary artery disease (CAD), myocardial infarction, angina pectoris, anginal equivalent, peripheral vascular disease, congestive heart failure, carotid stenosis)

- Severe hypertension (systolic blood pressure >180mmHg or diastolic blood pressure >105mmHg), even if well-controlled by medication.

- Diagnosed diabetes mellitus

- Regular use of multivitamins, Vitamin C, Vitamin E, fish oil, flax seed oil, omega-3 fatty acids, CoQ10, fiber supplements, garlic pills, arginine, red yeast rice, and any kind of antioxidant and unwillingness to discontinue supplementation for at least 4 weeks prior to study initiation and for study duration

- Allergic to walnuts or any other nuts

- Diagnosed eating disorder

- On any specific diet, weight control diet, vegan diet

- Any rheumatologic disease requiring regular use of NSAIDs or alternative medications

- Regular use of fiber supplements

- Regular use of vasoactive medication (including glucocorticoids, antineoplastic agents, psychoactive agents, or bronchodilators), and anticoagulant drugs (including Coumadin, plavix )

- Diagnosed sleep apnea

- Substance abuse (chronic alcoholism, other chemical dependency)

- Any unstable medical condition that would limit the ability of a subject to participate fully in the trial (e.g., cancer, AIDS, tuberculosis, psychotic disorder)

- Current or impending pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Walnut Supplementation
Eight weeks of walnut supplementation
No walnut supplementation
Eight weeks without walnut supplementation

Locations

Country Name City State
United States Yale-Griffin Prevention Research Center Derby Connecticut

Sponsors (2)

Lead Sponsor Collaborator
Griffin Hospital California Walnut Commission

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Endothelial function Brachial artery flow mediated dilation (FMD) 8 weeks
Secondary Weight 8 weeks
Secondary Waist circumference 8 weeks
Secondary Fasting lipid panel Total cholesterol, low density lipoprotein cholesterol, high density lipoprotein cholesterol, triglyceride level, cholesterol / high density lipoprotein cholesterol ratio 8 weeks
Secondary Fasting blood glucose 8 weeks
Secondary Fasting insulin 8 weeks
Secondary Blood pressure 8 weeks
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