Status
Conditions
Treatments
About
The purpose of this study is to evaluate the long-term safety and performance of complex endovascular aneurysm repair by inclusion in a longitudinal registry
Full description
This is a Global, multicenter, prospective, observational, non-randomized, single-arm, open clinical study will evaluate the long term (i.e. >5 years) safety and efficacy of complex endovascular repair
This study will enroll all patients treated with Fenestrated and Branched devices in Europe and Canada that follow all inclusion criteria and none of the exclusion criteria. The total duration of the study will be of approximately 7 years.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Inclusion criteria
A patient is deemed suitable for inclusion in the study if the patient meets both of the following criteria:
Exclusion criteria
Patients are excluded from enrolment into the study if any of the following are true:
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal