Viewing Study NCT00171769



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00171769
Status: COMPLETED
Last Update Posted: 2017-02-23
First Post: 2005-09-13

Brief Title: Atrial Fibrillation Feasibility Certoparin Trial - AFFECT
Sponsor: Novartis
Organization: Novartis

Study Overview

Official Title: An Open Label Multi-center Trial to Evaluate the Feasibility and Safety of Short-term Treatment With Subcutaneously Injected Certoparin 8000 U Anti-Xa Twice Daily in Patients With Persistent Nonvalvular Atrial Fibrillation
Status: COMPLETED
Status Verified Date: 2017-02
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: This trial is designed to provide data about feasibility and safety of short-term treatment with the low-molecular-weight heparin certoparin in patients with persistent nonvalvular atrial fibrillation
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