Evaluation of heart failure treatment guided by N-terminal pro b-type natriuretic peptide (NTproBNP) vs clinical symptoms and signs alone

Study identifier:D2452L00010

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

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

Medical condition

heart failure

Phase

Phase 4

Healthy volunteers

No

Study drug

Captopril, Enalapril, Lisinopril, Ramipril, Trandolapril, Bisoprolol, Carvedilol, Metoprolol succinate, Candesartan, Valsartan, Eplerenone, Spironolactone, Diuretics, HF treatment according to Swedish guidelines

Sex

All

Actual Enrollment

252

Study type

Interventional

Age

18 Years +

Date

Study Start Date: 01 Oct 2006
Primary Completion Date: 01 Jan 2009
Study Completion Date: 01 Jan 2009

Study design

Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment

Verification:

Verified 01 Jun 2012 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria