Dyslipidemia Clinical Trial
Official title:
Hepatic Lipase Variant -514 C/T in a High Fat vs. Low Fat Diet for Cardio-metabolic Outcomes: A Crossover Randomized Dietary Intervention Trial
Verified date | October 2016 |
Source | Tufts University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The investigators evaluated dietary modulation of LIPC rs1800588 (-514 C/T) for lipids and glucose using a randomized cross-over design comparing a high-fat Western diet and a low-fat traditional Hispanic diet in Caribbean Hispanics (n=42; 4 weeks/phase).
Status | Completed |
Enrollment | 42 |
Est. completion date | July 2012 |
Est. primary completion date | July 2012 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Self-reported Caribbean Hispanics Exclusion Criteria: - diabetes - uncontrolled hypertension - self-reported liver disease; severe kidney dysfunction; angina; endocrine disease; preexisting cardiovascular disease or gallbladder disease, or pancreatitis within the past 12 months - use of lipid-lowering or hypoglycemic medications - BMI >34 kg/m2 - alcohol consumption (>2 drinks/day) - smoking within the past 6 months or illegal drug use - pregnancy or breastfeeding - weight gain or loss of more than 9 kg within the past 6 months - extreme levels of physical or athletic activity, strict vegetarians/vegans - egg, wheat, milk, fish, or nut allergies - unwillingness to discontinue fish oil or flaxseed supplements or drinking alcohol during the study - travel plans precluding availability for the two 4-week study phases |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Tufts University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change in fasting high-density lipoprotein cholesterol | From date of randomization until completion of each 4 week dietary intervention | No | |
Secondary | change in fasting plasma triglycerides | From date of randomization until completion of the 4 week dietary intervention | No | |
Secondary | change in fasting plasma glucose | From date of randomization until completion of the 4 week dietary intervention | No | |
Secondary | oral glucose tolerance test | 2 hours post-oral glucose load | No | |
Secondary | post-prandial lipemia 4 hours | 4 hours post-oral fat load | No | |
Secondary | post-prandial lipemia 8 hours | 8 hours post-oral fat load | No |
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