Moderate Alcohol Intake Among Patients With Type 2 Diabetes

Sponsor
The S. Daniel Abraham International Center for Health and Nutrition (Other)
Overall Status
Unknown status
CT.gov ID
NCT00295334
Collaborator
The Israeli Diabetes Research Group (Other), Hadassah Medical Organization (Other), Soroka University Medical Center (Other), Julio Vainstein, Wolfson Medical Center, Holon, Israel (Other), Tishbi Wines, Israel and Admiral Wine Imports, US (Other), Harvard University (Other)
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Study Details

Study Description

Brief Summary

Our specific aim is to explore the effect of moderate alcohol intake on parameters of glycemic index and lipid profile among patients with type 2 diabetes.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Successful long-term control of hyperglycemia decreases the risk for diabetic complications . Although a family history of diabetes is an established risk factor for type 2 diabetes, lifestyle factors also play an important role in its cause . However, physicians are poorly informed about how their patients' alcohol use affects risk for or management of diabetes. Moderate alcohol consumption has been associated with lower risk of both cardiovascular disease and type 2 diabetes, and is also linked to lower cardiovascular risk among type 2 diabetics. Potential mechanisms have focused primarily on lipid metabolism, coagulation, fibrinolysis, and insulin sensitivity. A recent systematic review of the literature to assess the effect of alcohol consumption on risk for and management and complications of diabetes mellitus suggests that moderate alcohol consumption is associated with a decreased risk for diabetes, whereas heavy alcohol consumption may be associated with an increased risk. Our aim is to assess the effect of moderate alcohol intake on glycemic control and cardiovascular disease mediators among patients with type 2 diabetes.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Prevention
Study Start Date :
Feb 1, 2006
Study Completion Date :
Dec 1, 2006

Outcome Measures

Primary Outcome Measures

  1. adherence, HbA1c, Glc []

Secondary Outcome Measures

  1. LDL, HDL, TG []

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age between 40-75 yrs.

  2. Alcohol abstainers (less than or equal to 1 drink/week)

  3. Established diagnosis of type 2 diabetes.

  4. Clinically stable, with no stroke or MI within the last 3 months and no major surgery within the last 3 months.

Exclusion Criteria:
  1. Taking Insulin >2 injections /day, or with insulin pump.

  2. TGs>500 mg/dL.

  3. HbA1c >10%

  4. Serum creatinine > 2 mg/dl

  5. Liver dysfunction (above 2 fold level of ALT and/or AST enzymes)

  6. Evidence of severe diabetes complications (such as proliferative retinopathy or renal disease).

  7. Patients with autonomic neuropathy manifested as postural hypertension and/or hypoglycemia unawareness. 7. Using drugs that might significantly interact with moderate alcohol. List of drugs will be obtained from pharmacology expert. 8. Presence of active cancer, receiving or had received chemotherapy in last 3 years.

  8. Suffering a major illness that might probably require hospitalization (upon physician's evaluation).

  9. Clinically assessed as having high potential of addictive behavior as judged by a validated clinical assessment and/or personal or family history of addiction, alcoholism or alcohol abuse.

  10. Severe symptoms during run-in as assessed by the physician. 12. Pregnant or lactating women. 13. Participation in another trial in which active intervention is being received.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • The S. Daniel Abraham International Center for Health and Nutrition
  • The Israeli Diabetes Research Group
  • Hadassah Medical Organization
  • Soroka University Medical Center
  • Julio Vainstein, Wolfson Medical Center, Holon, Israel
  • Tishbi Wines, Israel and Admiral Wine Imports, US
  • Harvard University

Investigators

  • Principal Investigator: Iris Shai, RD PhD, Ben-Gurion University of the Negev

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00295334
Other Study ID Numbers:
  • 250505
First Posted:
Feb 23, 2006
Last Update Posted:
Sep 13, 2006
Last Verified:
Sep 1, 2006
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2006