Evaluation of Heart Failure Treatment Guided by N-terminal Pro B-type Natriuretic Peptide (NTproBNP) vs Clinical Symptoms and Signs Alone

NCT00391846 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 252

Last updated 2012-06-25

Study results available
· View outcomes & findings →

Summary

The purpose is to study if HF treatment guided by NTproBNP in addition to clinical symptoms and signs is more effective than treatment guided by clinical symptoms and signs alone in patients with HF and left ventricular systolic dysfunction

Conditions

Interventions

DRUG

Captopril

DRUG

Enalapril

DRUG

Lisinopril

DRUG

Ramipril

DRUG

Trandolapril

DRUG

Bisoprolol

DRUG

Carvedilol

DRUG

Metoprolol succinate

DRUG

Candesartan

DRUG

Valsartan

DRUG

Eplerenone

DRUG

Spironolactone

DRUG

Diuretics

DRUG

HF treatment according to Swedish guidelines

PROCEDURE

Blood samples

PROCEDURE

The Kansas City Cardiomyopathy Questionnaire (KCCQ)

Sponsors & Collaborators

Principal Investigators

  • AstraZeneca Sweden Medical Director, MD · AstraZeneca

  • Hans Persson, MD, PhD · Danderyd Hospital, Sweden

  • Bjorn Eriksson, MD · AstraZeneca

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-10-31
Primary Completion
2009-01-31
Completion
2009-01-31

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00391846 on ClinicalTrials.gov