Atrial Fibrillation
Conditions
Brief summary
Post Marketing study, Interventional, Prospective, non randomised Describe how the MD is using the information of the ICM in addition of standard FU(clinical exam and holter 24h)post AF ablation(1 year FU).
Interventions
DEVICEICM Implantation
Sub cutaneous implantation of the ICM
Sponsors
Dr Ange FERRACCI
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* AF thermoablation indication * Informed Consent signed, * Age between 18 & 75
Exclusion criteria
* Participation to other clinical trial * Non compliant patient * Pregnant women * Left Atrial thrombus * Endocarditis, infection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical exam and ECG record | one month, 3 months, 6 months , 12 months |
Countries
France
Outcome results
None listed