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Standardized Physician-modified Fenestrated Endograft Registry

Study acronym: SPHERE
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Eligibility criteria revised
    • Secondary endpoints: details revised at 1 of 2 entries
    • Study title revised
    • Study description expanded, about 2 words
    v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Multicenter retrospective study including all consecutive patients treated by PMEG using a standard modification technique of Valiant Captivia (Medtronic, Minneapolis, MN-USA).
Trial Details
NCT Number NCT06358248
Lead Sponsor University Hospital Padova
Conditions
(from sponsor)		 Aortic Aneurysm, Thoracoabdominal, Aortic Diseases
Related terms Aortic Aneurysm, Aortic Aneurysm, Thoracoabdominal, Aortic Diseases
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov