Glipizide and Metformin |
Metaglip |
Clinical Trial: The Effects of Metformin on Blood Vessel Structure and Function
This study is currently recruiting patients.
|
Purpose
The purpose of this study is to evaluate whether the drug Metformin has beneficial effects on the blood vessels of individuals with the Metabolic Syndrome (MeS).
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Obesity Hypertension Hypercholesterolemia Hyperglycemia | Drug: Metformin | Phase II |
MedlinePlus related topics: Cholesterol; High Blood Pressure; Metabolic Disorders; Obesity
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: The Effects of Metformin on Vascular Structure and Function in Subjects with the Metabolic Syndrome (MET Trial)
Expected Total Enrollment: 84
Study start: January 2004; Expected completion: June 2006
Individuals with the Metabolic Syndrome (MeS) are at increased risk for developing cardiovascular diseases. This increased risk may, in part, be related to abnormalities in the blood vessels. MeS is defined as having 3 or more of the following 5 criteria:
- Abdominal obesity (waist measurement >39.8 inches in men, >34.4 inches in women)
- Elevated triglycerides (>150 mg/dl)
- Low HDL or “good” cholesterol (<40 mg/dl in men or <50 mg/dl in women)
- Elevated blood pressure (>130/85) or treatment for high blood pressure
- Elevated fasting blood sugar (>100 mg/dl)
Metformin is a medication that is approved by the Food and Drug Administration (FDA) for the treatment of diabetes; however, it can also be safely administered to non-diabetic subjects. We are evaluating whether Metformin reduces the stiffness of blood vessels and improves endothelial function.
This study requires 4 visits to the NIA Clinical Research Center (located on the premises of Harbor Hospital) over a 5-month period. At the initial visit, patients will be given a physical examination with blood and urine tests, and an EKG. They will be randomized into one of two groups; one group will receive Metformin (1700 mg per day), while the other group will receive a placebo. Participants will take the medication for 4 months. Subsequent visits will include additional blood tests, ultrasound and echo exams.
Taking part in this study is entirely voluntary. All testing and medications will be provided at no cost to the participant or their family.
Eligibility
Ages Eligible for Study: 21 Years - 80 Years, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
Participants with the Metabolic Syndrome, which is defined as having 3 or more of the following 5 alterations:
- Abdominal obesity (waist measurement >39.8 inches in men, >34.4 inches in women)
- Elevated triglycerides (>150 mg/dl)
- Low HDL or “good” cholesterol (<40 mg/dl in men or <50 mg/dl in women)
- Elevated blood pressure (>130/85) or treatment for high blood pressure
- Elevated fasting blood sugar (>100 mg/dl)
Exclusion Criteria:
- Diabetes treated with medication
- Blood pressure >160/100 mmHg
- Clinical Congestive Heart Failure
- Anemia with hematocrit <32%
- Asthma or Chronic Obstructive Pulmonary Disease (COPD) requiring daily medication or use of home oxygen therapy
- Major surgery planned within the next six months
- A recent, unexplained weight loss of >10% of body weight in the past 6 months
- A known allergy or hypersensitivity to Metformin
- History of hepatitis or cirrhosis
- History of kidney disease (defined as serum creatinine >1.4 mg/dL in men, >1.3 mg/dL in women, or urine protein >2+)
- Pregnancy or the absence of an effective method of contraception
- Illicit drug or alcohol abuse
- Cancer requiring treatment currently or recently completed treatment in the last 2 months
Location and Contact Information
Maryland
National Institute on Aging (NIA), Harbor Hospital, Baltimore, Maryland, 21225, United States; Recruiting
Sarah Betkey, Participant Recruitment 410-350-3941or 800-225-2572 Ext. 3941 betkeys@grc.nia.nih.gov
Samer S. Najjar, MD, Principal Investigator
Samer S. Najjar, MD, Principal Investigator, Staff Clinician - NIA, NIH
More Information
Publications
Knowler WC, Barrett-Connor E, Fowler SE, Hamman RF, Lachin JM, Walker EA, Nathan DM; Diabetes Prevention Program Research Group. Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N Engl J Med. 2002 Feb 7;346(6):393-403.
Beisswenger PJ, Howell SK, Touchette AD, Lal S, Szwergold BS. Metformin reduces systemic methylglyoxal levels in type 2 diabetes. Diabetes. 1999 Jan;48(1):198-202.
Mather KJ, Verma S, Anderson TJ. Improved endothelial function with metformin in type 2 diabetes mellitus. J Am Coll Cardiol. 2001 Apr;37(5):1344-50.
[No authors listed] Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). UK Prospective Diabetes Study (UKPDS) Group. Lancet. 1998 Sep 12;352(9131):854-65. Erratum in: Lancet 1998 Nov 7;352(9139):1557.
Record last reviewed: March 2005
Last Updated: March 3, 2005
Record first received: March 3, 2005
ClinicalTrials.gov Identifier: NCT00105066
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Glipizide and Metformin (Drug Digest)
- Metaglip (Drug Digest)

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