Clinical Trials Directory

Trials / Completed

CompletedNCT02543281

Adaptive CRT Effect on Electrical Dyssynchrony

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Larisa Tereshchenko · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to better understand how adaptive cardiac resynchronization therapy (aCRT) might benefit patients. aCRT works by sometimes giving stimulation to only the left side of the heart, rather than to both sides, depending on how it senses the heart is functioning. CRT without the adaptive algorithm works by giving stimulation to both sides of the heart. aCRT has already been approved by the FDA and is being used in patients now, but it is not clear which patients it should be used in compared to normal CRT. This study will include patients who are already scheduled to get a CRT device. The investigators will then randomize patients to the aCRT study arm or to the CRT study arm. After 6 months, the investigators will assess the electrical activity of the patients' hearts. After this time, the patient and their doctors will be able to decide if they would like to change the type CRT they have been designated.

Conditions

Interventions

TypeNameDescription
DEVICEAdaptive cardiac resynchronization therapyThe adaptive cardiac resynchronization therapy (aCRT) algorithm works by sometimes giving stimulation to only the left side of the heart, rather than to both sides, depending on how it senses the heart is functioning.
DEVICEConventional Cardiac Resynchronization TherapyCRT without the adaptive algorithm works by giving stimulation to both sides of the heart.

Timeline

Start date
2015-04-01
Primary completion
2021-09-01
Completion
2021-09-01
First posted
2015-09-07
Last updated
2025-03-20
Results posted
2023-11-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02543281. Inclusion in this directory is not an endorsement.