Study identifier:D2452L00010
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A randomised, single blind, multicentre, 9-month, phase IV study, comparing treatment guided by clinical symptoms and signs and NT-proBNP vs treatment guided by clinical symptoms and signs alone, in patients with heart failure (HF) and left ventricular systolic dysfunction
heart failure
Phase 4
No
Captopril, Enalapril, Lisinopril, Ramipril, Trandolapril, Bisoprolol, Carvedilol, Metoprolol succinate, Candesartan, Valsartan, Eplerenone, Spironolactone, Diuretics, HF treatment according to Swedish guidelines
All
252
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment
Verified 01 Jun 2012 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
Other: Guided by NT-proBNP Treatment guided by clinical symptoms and signs + NTproBNP | - |
Other: Not Guided by NT-proBNP Treatment guided by clinical symptoms and signs | - |