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Clinical Assessment of Essential Remote Monitoring Functions in Pacemakers — CALLIOPE  

Bradycardia Clinical Trial

Official title:
Clinical Assessment of Essential Remote Monitoring Functions in Pacemakers

Clinical Trial Summary

The purpose of the clinical investigation is to document the safety and the performances of the remote monitoring functions of the ALIZEA, BOREA and CELEA pacemakers, i.e. the RAAT, the RVAT and the remote alerts.

Clinical Trial Description

All patients will be included just after implantation and will then be followed during 48 months after inclusion. At each on-site or remote follow-up visit (1 to 3 months, 6, 12, 24 and 48 months), performances of the remote monitoring functions and the cardiac pacing system itself will be measured, and safety will be monitored during the whole clinical investigation duration. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05165095
Study type Observational
Source MicroPort CRM
Contact Antoine Guihard
Phone +33 1 46 01 33 20
Email antoine.guihard@crm.microport.com
Status Recruiting
Phase
Start date March 25, 2022
Completion date July 2027
View Details
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