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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00515476
Other study ID # 4031215
Secondary ID
Status Completed
Phase N/A
First received August 9, 2007
Last updated June 22, 2010
Start date June 2007
Est. completion date December 2008

Study information

Verified date November 2009
Source Hannover Medical School
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Interventional

Clinical Trial Summary

The purpose of the present study is to characterize the quality of HDL-Cholesterol in patients with metabolic syndrome and reduced blood HDL-Cholesterol levels and to examine the effect of exercise training on the vasculoprotective effects of HDL-Cholesterol in these patients. Additionally the investigators aim to investigate the endothelial function, oxidative stress and the regenerative capacity of the endothelial progenitor cells in patients with metabolic syndrome and the changes dependent on physical activity of patients.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date December 2008
Est. primary completion date November 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 21 Years to 75 Years
Eligibility Inclusion Criteria:

- Reduced HDL-Cholesterol levels in blood: < 40 mg/dl (1.03 mmol/L) in male, < 50 mg/dl (1.29 mmol/L) in female

- Plus two of the following criteria:

- Elevated waist circumference: = 102 cm (= 40 inches) in men or = 88 cm (= 35 inches) in women

- Elevated triglycerides: = 150 mg/dL (1.7 mmol/L

- Elevated blood pressure: = 130 mmHg systolic blood pressure or = 80 mmHg

- diastolic blood pressure or anti-hypertensive treatment

- Elevated fasting glucose: = 100 mg/dL or on drug treatment for elevated fasting glucose

Exclusion Criteria:

- Acute coronary syndrome

- Unstable Angina pectoris

- Myocardial infarction during the last 8 weeks

- Therapy with Niacin

- Active infections

- Ventricular arrhythmias

- Systolic blood pressure > 160 mmHg or diastolic blood pressure > 95 mmHg

- Cancer

- Pregnancy, lactation

- Alcoholism

Study Design

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


Related Conditions & MeSH terms


Intervention

Behavioral:
physical exercise
8 weeks of regular exercise training

Locations

Country Name City State
Germany Hannover Medical School Hannover

Sponsors (1)

Lead Sponsor Collaborator
Hannover Medical School

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary: vasculoprotective and regenerative functions of HDL-Cholesterol and EPC function before and after 8-weeks exercise training before and after 8-weeks exercise training No
Secondary Secondary: flow-mediated, endothelium-dependent vasodilation of radial artery measured by ultrasound before and 8 weeks after exercise training No
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