Clinical Trials Directory

Trials / Completed

CompletedNCT00746135

TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study

TRI-V Resynchronization in Paced Heart Failure Patients With ICD Indication.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Abbott Medical Devices · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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).

Conditions

Interventions

TypeNameDescription
DEVICEDevice ImplantationRV apical pacing lead, RV pacing lead at HIS bundle position, LV pacing lead implantation

Timeline

Start date
2007-11-01
Primary completion
2010-10-01
Completion
2012-12-01
First posted
2008-09-03
Last updated
2019-02-04

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00746135. Inclusion in this directory is not an endorsement.

TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study (NCT00746135) · Clinical Trials Directory