Clinical Trials Directory

Trials / Completed

CompletedNCT01798797

Integrated Diagnostic for Heart Failure

Status
Completed
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
Medtronic · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A prospective post-market study to evaluate the performance and clinic usability of heart failure risk status (HFRS) feature on CareLink.

Detailed description

Patients with systolic heart failure (HF) implanted with Medtronic wireless implantable cardiac defibrillator (ICD) or cardiac resynchronization therapy device with defibrillation capabilities (CRT-D) devices will be enrolled in the study. The purpose of the study is to evaluate the usability of CareLink HFRS to manage a patient's heart failure.

Conditions

Timeline

Start date
2013-08-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2013-02-26
Last updated
2018-09-25

Locations

3 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT01798797. Inclusion in this directory is not an endorsement.

Integrated Diagnostic for Heart Failure (NCT01798797) · Clinical Trials Directory