Viewing Study NCT00501722



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Last Modification Date: 2024-10-26 @ 9:34 AM
Study NCT ID: NCT00501722
Status: COMPLETED
Last Update Posted: 2009-01-12
First Post: 2007-07-13

Brief Title: Satavaptan Dose-Ranging Study in Hyponatraemic Patients With Cirrhotic Ascites
Sponsor: Sanofi
Organization: Sanofi

Study Overview

Official Title: SR121463B in Cirrhotic Ascites Treatment With Hyponatraemia A Placebo-Controlled Dose-Comparison Study
Status: COMPLETED
Status Verified Date: 2009-01
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: HypoCAT
Brief Summary: The primary objective is to determine the optimal dose or range of doses of SR121463B for the treatment of ascites and the correction of hyponatraemia when used concomitantly with a standard dose regimen of spironolactone

The secondary objective is to determine the tolerability of different fixed doses of SR121463B over a 14 day treatment period in cirrhotic ascites

This HypoCAT study is followed by a single-blind placebo-controlled one-year long-term safety extension ExpoCAT The first extension is followed by another long-term study PASCCAL-1
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
LTS10209 None None None
LTS5634 None None None