Overview

Nt-proBNP Guided Primary Prevention of CV Events in Diabetic Patients

Status:
Completed
Trial end date:
2011-12-01
Target enrollment:
0
Participant gender:
All
Summary
Increased levels of NT-proBNP are known to increase the risk of cardiac events in diabetic patients. The other way around, patients with normal values have an excellent prognosis on short-term. We intend in our study to proof the hypothesis, whether it is possible to decrease NT-proBNP levels by intensified cardiac prevention care We aim those patients, who already have elevated levels, although no history of a cardiac disease. This decrease in NT-proBNP should be translated consequently in a decrease in cardiac events
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Medical University of Vienna
Collaborator:
Roche Pharma AG
Treatments:
Bisoprolol
Telmisartan
Criteria
Inclusion Criteria:

- Age > 18 years

- Known Diabetes mellitus > 6 months

- Increased Nt-proBNP above 125pg/ml

- Given informed consent

Exclusion Criteria:

- Disease other than diabetes, with a life expectancy below 1 year

- patients who suffer from chronic infection or malignant disease

- Women in childbearing age without contraceptive

- History of cardiac disease

- systemic cortisone treatment

- patients who are on chronic or acute hemodialysis, ultra filtration or peritoneal
dialysis