EVAR
ProcedureBranch Evar with the e-liac device
NCT Number: NCT06946381
Spontaneus Multicentric Observational registry to investigate the medium and long-term performances of the Iliac E-liac Branch Device from Artivion for treatment of Aortoiliac aneurysms in a real-world consecutive patients cohort.
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Observational
Azienda ospedaliero-universitaria consorziale policlinico di Bari, Bari, BA, Italy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Branch Evar with the e-liac device
Time frame: assessed after procedure at 30 days, 6 months, one year, two years, three years, four years, five years.
Aneurysm related death
Time frame: assessed after procedure at 30 days, 6 months, one year, two years, three years, four years, five years
Procedure-related re intervention
Time frame: assessed after procedure at 30 days, 6 months, one year, two years, three years, four years, five years
Variation in aneurysm sac diameter
Contact information is provided by the study sponsor or research team.
Federico II University
Other
Acronym: CAMPARI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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