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Recruiting NCT06358248

NCT06358248 Standardized Physician-modified Fenestrated Endograft Registry

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Clinical Trial Summary
NCT ID NCT06358248
Status Recruiting
Phase
Sponsor University Hospital Padova
Condition Aortic Aneurysm, Thoracoabdominal
Study Type OBSERVATIONAL
Enrollment 50 participants
Start Date 2023-10-01
Primary Completion 2028-10-01

Trial Parameters

Condition Aortic Aneurysm, Thoracoabdominal
Sponsor University Hospital Padova
Study Type OBSERVATIONAL
Phase N/A
Enrollment 50
Sex ALL
Min Age 18 Years
Max Age 100 Years
Start Date 2023-10-01
Completion 2028-10-01
Interventions
Physician-modification of Valiant Captivia Endograft (Medtronic, Minneapolis, MN-USA).

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Brief Summary

Multicenter retrospective study including all consecutive patients treated by PMEG using a standard modification technique of Valiant Captivia (Medtronic, Minneapolis, MN-USA).

Eligibility Criteria

INCLUSION CRITERIA * Complex AAA (including short-neck AAA, JRAA, PRAA, extent IV TAAA) * Haemodynamic stability * Anatomical feasibility is based on the presence of a proximal aortic neck above the mid celiac trunk of ≥25 mm in length and between 18 mm and 35 mm in diameter; the neck needs to be "healthy" with no parietal calcifications or thrombus with a cylindrical shape. The visceral aorta is required to be no larger than 40 mm in maximum diameter. EXCLUSION CRITERIA * Extent I-III TAAA * Hemorrhagic shock

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