ProMRI ICD/CRT-D Post Approval Study

Biotronik

Status: Completed

Conditions: Tachyarrhythmia

Study type: Observational

Funder types: Industry

Identifiers

NCT02933619

ProMRI PAS

Details and patient eligibility

About

Following product approval, confirmation of appropriate VF episode detection after MRI exposure of the ProMRI ICD/CRT-D systems and to evaluate left ventricular pacing threshold changes post-MRI.

Enrollment: 24,249 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• ProMRI ICD/CRT-D system enabled with BIOTRONIK Home Monitoring.

Exclusion criteria

• None