Viewing Study NCT00746135


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Study NCT ID: NCT00746135
Status: COMPLETED
Last Update Posted: 2019-02-04
First Post: 2008-08-20
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study
Sponsor: Abbott Medical Devices
Organization:

Study Overview

Official Title: TRI-V Resynchronization in Paced Heart Failure Patients With ICD Indication.
Status: COMPLETED
Status Verified Date: 2019-01
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: TRI-V
Brief Summary: It's the aim of this study to investigate the impact of Right Ventricular (RV) lead position (RV-apex, His bundle area, RV-apex+His bundle area) in combination with individually optimized Left Ventricular (LV) lead placement and CRT timing on the outcome of cardiac resynchronization therapy (CRT).
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: