Alcohol and Atherosclerosis Pilot Study (AAAPILOT)
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|ClinicalTrials.gov Identifier: NCT00786279|
Recruitment Status : Completed
First Posted : November 6, 2008
Last Update Posted : January 12, 2016
|Condition or disease||Intervention/treatment||Phase|
|Atherosclerosis||Other: ethanol Other: Ethanol-free beverage||Not Applicable|
The feasibility of a long-term randomized trial of alcohol intake on clinical endpoints is uncertain. One approach that could minimize the size and duration of such a randomized trial would be to assess the effect of alcohol on progression of radiologically-defined atherosclerosis.
We propose a proof-of-principle pilot study of the effect of longer-term alcohol intake on atherosclerosis. We will recruit and randomize 40 participants aged 55 and older at high risk for CHD to a six-month period of consumption of a single 150 ml glass per day of either 10% ethanol (approximating wine) or water. At baseline and after 6 months, we will assess aortic atherosclerosis using magnetic resonance imaging. We will determine adherence in several ways, including serum markers, dietary recalls, and measurement of unused beverage. The primary outcomes in this feasibility study will be compliance with alcohol intake and the two MRI examinations. As secondary outcomes, we will measure standard and novel cardiovascular risk markers, including inflammatory markers and measures of glucose metabolism. We will assess safety on a continual basis, including repeated testing of liver enzymes and blood counts.
If successful, this pilot study will form the basis for a more definitive trial to determine the effect of alcohol intake on progression of atherosclerosis, which could itself establish the feasibility of even larger, longer-term studies of alcohol intake and occurrence of cardiovascular events.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||39 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||Alcohol and Atherosclerosis Pilot Study|
|Study Start Date :||November 2008|
|Actual Primary Completion Date :||March 2011|
|Actual Study Completion Date :||April 2015|
Placebo Comparator: 1
150 cc daily of flavored, calorie-free beverage without alcohol
Other: Ethanol-free beverage
0 grams ethanol daily for 6 months.
150 cc flavored, calorie-free beverage with 15 gm ethanol daily
15 gm ethanol daily for 6 months
- Adherence to alcohol intake and MRI examinations [ Time Frame: 6 months ]
- GGT [ Time Frame: Monthly ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00786279
|United States, Massachusetts|
|Beth Israel Deaconess Medical Center|
|Boston, Massachusetts, United States, 02215|
|Principal Investigator:||Kenneth J. Mukamal, MD, MPH||Beth Israel Deaconess Medical Center|