Viewing Study NCT00303498



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Last Modification Date: 2024-10-26 @ 9:23 AM
Study NCT ID: NCT00303498
Status: COMPLETED
Last Update Posted: 2023-01-04
First Post: 2006-03-16

Brief Title: A Study of the Effectiveness of Sitaxsentan Sodium in Patients With Diastolic Heart Failure
Sponsor: Pfizer
Organization: Pfizer

Study Overview

Official Title: A PHASE 2 RANDOMISED DOUBLE-BLIND PLACEBO-CONTROLLED EXPLORATORY EFFICACY STUDY OF SITAXSENTAN SODIUM TO IMPROVE IMPAIRED EXERCISE TOLERANCE IN SUBJECTS WITH DIASTOLIC HEART FAILURE
Status: COMPLETED
Status Verified Date: 2022-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study was to determine whether long-term 6 months at the target dose blockade of ETA receptors using sitaxsentan showed functional benefit in subjects with chronic Heart Failure and an Left Ventricular Ejection Fraction 50
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
FDHF01 OTHER Alias Study Number None