Bradycardia Risk Stratification With Loop Recorder After Syncope

Central Hospital, Nancy, France

Status: Unknown

Conditions: Implantable Loop Recorder

Study type: Observational

Funder types: Other

Identifiers

NCT04200014

2019PI198

Details and patient eligibility

About

Syncope is a common symptom that may be related to a conductive disorder. If no bradycardia is authenticated, it is often necessary to implant an implantable loop recorder.

In somes cases, implantable loop recorder records cardiac conductive disorders. In this study, we want to try to identify a group of patients for whom we could immediately implant a pacemaker without prior implantation of an implantable loop recorder given the high probability of implantation of a pacemaker after interrogation of the implantable loop recorder. It would be interesting for the reduction of interventions for the patients and for the economic aspect of the healthcare system

Enrollment: 250 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• All patients who have benefited from an Implantable Loop recorder in the Nancy's Teaching Hospital

Exclusion criteria

• No Exclusion Criteria

Trial design

250 participants in 1 patient group

Syncope and Implantable loop recorder

Description:

Patients implanted with a subcutaneous Loop Recorder after syncope in Nancy University Hospital