Atrial Septal Defect
Conditions
Keywords
IRFACODE II, ASD closure, ASD device, erosion, arrhythmia
Brief summary
The IRFACODE II study will evaluate the performance and safety of the Occlutech® Flex II device in patients with closure of secundum atrial septal defects (ASD II).
Detailed description
Introduction: Interventional ASD closure is generally a safe procedure with only a small amount of severe side effects including mainly erosion of the atrial wall, embolizations and arrhythmias. The IRFACODE study has shown excellent results in Patients with various generations of the Occlutech devices. IRFACODE II study will evaluate the performance and safety of the Occlutech® Flex II device in patients with closure of secundum atrial septal defects (ASD II). Methods: The IRFACODE II study is a retrospective, non-randomized open access study for centres with a minimum of about 50 patients to evaluate the safety and side effects of ASD closure with this device. A minimum of 2000 patients that have an ASD II closed with this device until 31. June 2016 will be enrolled, the follow-up will be until 31. June 2017. Primary outcome measures for safety are the amount of erosions over a minimum follow-up time of 12 months. Primary outcome measures for device performance will include the success of complete ASD closure. Secondary outcome measures for safety will include the technique of implantation, the success rate in anatomically difficult ASDs, the incidence of arrhythmias (AV block, atrial fibrillation or flutter), device embolization, embolic events or migraine. A subgroup analysis according to patients age and anatomy of the defect will be performed. Outlook: The IRFACODE II study is the first trial intended to detect the actual incidence of erosion after ASD closure using the Flex II device. Although the trial is primarily designed to study the safety and device performance, the incidence of other potential side effects will be also evaluated.
Interventions
DEVICEASD closure with the Occlutech Flex II ASD closure device
Monitoring of possible device related side effects with a minumum of 1 year follow-up.
Sponsors
Ludwig-Maximilians - University of Munich
Study design
Observational model
COHORT
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
ASD for device closure \-
Exclusion criteria
* life expectancy \< 12 months * participating in another study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| number of erosions | minimum 1 year | detection of erosions of the atrial wall after ASD closure |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| number of arrhythmias | minimum 1 year | detection of arrhythmias after ASD closure |
| successful implantation | minimum 1 year | number of successful device implantations after device was placed inside the heart |
| embolization | minimum 1 year | number of events of device embolization during Implantation and follow-up |
Outcome results
None listed