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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00558935
Other study ID # 24/06
Secondary ID
Status Terminated
Phase N/A
First received November 14, 2007
Last updated May 9, 2011
Start date October 2007
Est. completion date December 2008

Study information

Verified date May 2011
Source Bayside Health
Contact n/a
Is FDA regulated No
Health authority Australia: Human Research Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effects of red wine on ABCA1 levels


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date December 2008
Est. primary completion date October 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Healthy participants

- Aged 18-65 years

- Free of overt coronary disease

- BMI < 35

- Fasting plasma glucose <6.1 mmol

- Unmedicated

- No major illness

Exclusion Criteria:

- Unable to give informed consent

- Smokers

- Participants with alcoholism

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Red Wine
20g alcohol daily/red wine for 4 weeks

Locations

Country Name City State
Australia Baker Heart Research Institute Melbourne Victoria

Sponsors (1)

Lead Sponsor Collaborator
Bayside Health

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary measurements of dyslipidemia 2 years
Secondary lipid functionality 2 years
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