Reduction or Extension of COnduction Time With Ventricular Electromechanical Remodeling (RECOVER)

Samsung Medical Center

Status

Enrolling

Conditions

Heart Failure

Treatments

Diagnostic Test: Device interrogation

Study type

Observational

Funder types

Other

Industry

Identifiers

NCT04397224

2018-05-073

Details and patient eligibility

About

This prospective multicenter registry study aims to detect the serial changes in ventriculo-ventricular conduction times according to cardiac-resynchronization therapy response.

Enrollment

100 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

meeting the current ESC or ACCF/AHA/HRS Class I or Class IIa indications for cardiac-resynchronization (CRT) implant

Exclusion criteria

Myocardial infarction, unstable angina within 40 days prior the enrollment
Recent cardiac revascularization in the 4 weeks prior to the enrollment or planned for the 3 months following
Cerebrovascular accident (CVA) or transient ischemic attack (TIA) in the 3 months prior to the enrollment
Primary valvular disease requiring surgical correction
Pregnant or are planning during the duration of the investigation
Status 1 candidate for cardiac transplantation or consideration for transplantation over the next 12 months
Post-cardiac transplantation
Life expectancy < 12 months
Currently participating in any other clinical investigation except for observational registry