DIABETES MELLITUS TYPE 2 Clinical Trial
— WALNUTOfficial title:
Effects of Walnut Consumption on Endothelial Function in Type 2 Diabetes: A Randomized, Controlled, Cross-over Trial
| NCT number | NCT00901043 |
| Other study ID # | 2007-10 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | October 2007 |
| Est. completion date | September 2008 |
| Verified date | March 2020 |
| Source | Griffin Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to examine the effects of sustained walnut consumption on endothelial function and lipid markers in patients with Type 2 diabetes mellitus.
| Status | Completed |
| Enrollment | 24 |
| Est. completion date | September 2008 |
| Est. primary completion date | July 2008 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 35 Years to 75 Years |
| Eligibility |
Inclusion Criteria: 1. men and women ages 35-75 2. non-smoker 3. able to have blood pressure taken bilaterally 4. diagnosed with type 2 diabetes by physician for at least one year 5. stable glucose levels and medication dose for the past 3 months 6. not on insulin therapy Exclusion Criteria: 1. failure to meet inclusion criteria 2. anticipated inability to complete or comply with study protocol for any reason (e.g., inability to communicate in English, dementia) or any unstable medical condition that would limit the ability of a subject to participate fully in the trial (e.g., wasting illness, AIDS, tuberculosis, psychotic disorder) 3. diagnosed eating disorder 4. use of lipid-lowering or antihypertensive medications (statins, red rice yeast extract, garlic) unless stable on medication for at least 3 months and willing to refrain from taking medication for 12 hours prior to endothelial function (EF) scanning, vasoactive medication (i.e., glucocorticoids, antineoplastic agents, psychoactive agents, or bronchodilators) or nutriceuticals 5. regular use of multivitamins and/or complementary or alternative supplement therapy and unwillingness to discontinue supplementation for at least 8 weeks prior to study initiation and for study duration 6. any rheumatologic disease requiring regular use of nonsteroidal antiinflammatory drug (NSAIDs) or alternative medications 7. regular use of fiber supplements 8. preexisting cardiovascular disease, including symptomatic coronary artery disease (CAD), myocardial infarction, angina pectoris, anginal equivalent, peripheral vascular disease (claudication, amputation, or revascularization) congestive heart failure, carotid stenosis, aortic stenosis or stroke; diabetes, sleep apnea, severe uncontrolled hypertension (systolic blood pressure > 180 mmHg or diastolic blood pressure > 105 mmHg) 9. coagulopathy, known bleeding diathesis or history of clinically significant hemorrhage; current use of warfarin 10. clinically significant anemia (Hct < 36% in men, < 33% in women) 11. intestinal or stomach disease 12. inability to use right or left arm for endothelial function testing for any reason such as breast surgery, trauma, radiation to right axilla, lymphedema, right arm shunt, severe vascular disease in right arm 13. subjects on a disease specific diet 14. subjects on a weight control diet 15. subjects on a vegan diet 16. allergy to any kind of nut, including walnuts and peanuts |
| Country | Name | City | State |
|---|---|---|---|
| United States | Griffin Hospital | Derby | Connecticut |
| Lead Sponsor | Collaborator |
|---|---|
| Griffin Hospital | California Walnut Commission |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Brachial artery flow mediated dilation (FMD) | 8 weeks | ||
| Secondary | Change in weight, waist circumference, blood pressure, fasting lipids, fasting insulin, HBA1c and glucose levels | 8 weeks |
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