Post-market Surveillance of Micorport CRM Cardiac Implantable Electronic Devices
Recruiting · NCT05694572 · Observational (researchers observe without assigning treatment) · Lead sponsor: MicroPort CRM
View the official record on ClinicalTrials.gov →Interventions studied
Implantation of a CIED
What this trial is about
The primary objective of the study is to assess the chronic safety of MicroPort CRM market-released systems.
Who can take part
Age range
18 Years to 90 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Subjects who meet all the following criteria at the time of the inclusion visit may be enrolled in the study:
- Subject implanted with one of the following MicroPort CRM market-released system:
- ENO, TEO, OTO, ALIZEA, BOREA, or CELEA PM single chamber (SR) or dual chamber (DR) implanted after 01 January 2020 in combination with at least one XFINE or VEGA pacing lead
- ULYS, EDIS ICD single chamber (VR) or dual chamber (DR) system in combination with an INVICTA defibrillation lead. Additional XFINE or VEGA atrial pacing lead is optional.
- GALI CRT-D implanted in combination with an INVICTA defibrillation lead. Additional NAVIGO left ventricular pacing lead is optional.
- GALI SONR CRT-D in combination with an INVICTA defibrillation lead and with either a NAVIGO left ventricular or a SONRTIP atrial pacing lead.
- Future generation of market approved MicroPort CRM PM, ICD or CRT-D device associated with existing or future generation of MicroPort CRM lead
- Subject equipped with Remote Monitoring System (RMS) (only for subject implanted with ICD or CRT-D system)
- Subject followed yearly per standard practice by investigational site: in-clinic visit or remote visit through remote monitoring system
- Subject reviewed, signed and dated the Informed Consent Form (ICF) if applicable per country regulation
Exclusion criteria
- Subjects who meet any of the following criteria are not eligible to be enrolled in the study:
- Age less than 18 years old or more than 90 years at time of inclusion, incapacitated or under guardianship or kept in detention
- Life expectancy less than 1 year
- Currently enrolled in an active study of MicroPort CRM
Where it is running
1 location listed.
- Hospital Santa Marta Lisboa - Lisbon, Portugal