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Completed Phase 3 Interventional

Tezosentan in the Treatment of Acute Heart Failure

ClinicalTrials.gov ID: NCT00524433

Public ClinicalTrials.gov record NCT00524433. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 12:42 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel Group Study to Assess the Efficacy, Safety, and Tolerability of Tezosentan in Patients With Acute Heart Failure.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The randomized patients with acute heart failure will be stratified based on the presence or absence of a Swan-Ganz catheter and assigned to receive either tezosentan 5 mg/h for the first 30 minutes and 1 mg/h thereafter or matching placebo in a 1:1 manner. The duration of the treatment is 24 hours up to 72 hours. The duration of the follow-up period is 30 days after treatment initiation for death, re-hospitalizations and SAEs followed by a follow-up period of 5 months for vital status.

Study identification

NCT ID
NCT00524433
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Idorsia Pharmaceuticals Ltd.
Industry
Enrollment
713 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2003 (Type not available)
Primary completion
Jan 2005 (Actual)
Completion
Jan 2005 (Actual)
Last update posted
Jul 10, 2018

2003 – 2005

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Oracle Research Huntsville Alabama — —
USC Medical Center Los Angeles California — —
Jacksonville Center for Clinical Research Jacksonville Florida — —
University of Miami-Jackson Memorial Hospital Miami Florida — —
University Hospital Augusta Georgia — —
University of Iowa Hospital and Clinics Iowa City Iowa — —
Medical Research Institute Slidell Louisiana — —
Baystate Medical Center-Cardiology Section Springfield Massachusetts — —
Elmhurst Hospital Center Elmhurst New York — —
Columbia Presbyterian Medical Center-Heart Failure Center New York New York — —
New York University School of Medicine New York New York — —
University of North Carolina Chapel Hill North Carolina — —
Duke University Medical Center Durham North Carolina — —
LeBauer Cardiovascular Research Foundation Greensboro North Carolina — —
Baylor College of Medicine - Texas Medical Center Houston Texas — —
University of Texas, MD Anderson Cancer Center Houston Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00524433, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 10, 2018 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00524433 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →