Cardiac Autonomic Neuropathy in Patients With Metabolic Syndrome

Metabolic Syndrome Clinical Trial

— CAN  

Official title:

Cardiac Autonomic Neuropathy in Patients With Metabolic Syndrome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00907127
• Other study ID #: UM-5428
• Secondary ID: ADA
• Status: Completed
• Phase: Phase 1
• First received: May 20, 2009
• Last updated: December 13, 2013
• Start date: January 2007
• Est. completion date: December 2011

Study information

• Verified date: December 2013
• Source: University of Michigan
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The study will test whether damage of the heart nerves appears in patients before they develop diabetes.

Description:

Patients who have mild abnormalities of blood sugar, high blood pressure, abnormal lipids and/or obesity can have a condition called metabolic syndrome. These patients are at high risk for diabetes and Cardiac Autonomic Neuropathy (CAN). Subjects with diagnosed metabolic syndrome will be expected to participate in the Metabolic Fitness Program which is a University of Michigan diet exercise program located in the Cardiology department at Domino Farms in Ann Arbor. Time required for this program and the study is 6 months. Clinic visits will involve Cardiac autonomic testing (CAN) procedures, PET scans and labs which will measure pre and post program intervention.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: December 2011
• Est. primary completion date: December 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Subjects must have IGT or IFG and two other criteria of metabolic syndrome as defined by ATP III (IFG=fasting glucose = 100 mg/dl (5.5 mmol/l))

2. Definition of IGT/IFG: IGT/IFG will be defined based on the ADA diagnostic guidelines following an oral glucose tolerance test (OGTT) [2].

3. Other Required Criteria (2 of the following):

• Waist circumference = 102 cm (40 inches) in men and = 88 cm (35 inches) in women, {for Asian-Americans: men = 88 cm (35 inches), women = 78 cm (31 inches)}

• Triglycerides = 150 mg/dl (1.7 mmol/l) - patients on drug treatment with fibrates or nicotinic acid will be presumed to have triglycerides = 150mg/dl and low HDL

• HDL cholesterol < 40 mg/dl (1.0 mmol/l) in men and < 50 mg/dl (1.3 mmol/l) in women,

• Blood pressure = 130/= 85 mmHg

4. Age 18-65

5. Women of childbearing potential must be using contraception to prevent pregnancy

Exclusion Criteria:

1. Patients either pregnant or planning to become pregnant will be excluded

• Women of childbearing potential will have a urine pregnancy test as part of the screening visit

• Subjects who become pregnant during the study will undergo an exit visit and management of their IGT and Metabolic Syndrome will be returned to their primary care provider

2. Subjects with pre-existing cardiovascular disease including:

• myocardial infarction

• congestive heart failure

• known arrhythmias

• ventricular structural abnormalities and valvular disease

• peripheral vascular disease

3. Subjects with hypoxemic lung or heart disease

4. Subjects with established diabetes

5. Laboratory evidence for a disease known to cause neuropathy within 3 months of screening will be an exclusion (those without known abnormality or those with a remote abnormality (> 3 months) will undergo the serologic screening)

6. Significant neurological disease (e.g., Parkinson's disease, epilepsy, recent stroke)

7. Subjects taking drugs which interfere with the uptake or metabolism of catecholamines

8. Subjects with known history of chronic kidney disease or who have significant hepatic disease (AST, ALT > 3 times upper limit for normal) or a history of previous kidney, pancreas or cardiac transplantation.

9. Subjects having taken systemic investigational drugs within the last 6 months

10. Inability or unwillingness of subject or legal guardian/representative to give written informed consent

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

• Metabolic Syndrome
• Metabolic Syndrome X
• Nervous System Diseases
• Syndrome

Intervention

Behavioral:
• Exercise and Diet (Metabolic Fitness Program)
6 month program of diet and exercise training and support.

Locations

Country	Name	City	State
United States	The University of Michigan Health System	Ann Arbor	Michigan

Sponsors (2)

Lead Sponsor	Collaborator
University of Michigan	American Diabetes Association

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cardiac autonomic testing (CAN)		6 months	No
Secondary	PET Scan		6 month	No