Monocentric Retrospective Observational Study; Analysis of Gore Excluder ACS Device Using Numerical Simulation
NCT ID: NCT06428877
Last Updated: 2024-05-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
20 participants
OBSERVATIONAL
2023-06-15
2024-04-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Patients who underwent EVAR with ACS Gore excluder.
Patients who underwent EVAR with ACS Gore excluder. Only patients with proximal neck angulation superior to 60 degrees will be considered.
analyzed on the post-operative scanner
analyzed on the post-operative scanner
Interventions
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analyzed on the post-operative scanner
analyzed on the post-operative scanner
Eligibility Criteria
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Inclusion Criteria
1. Is age ≥18 at the time of inclusion.
2. Underwent EVAR with ACS Gore Excluder
3. AAA proximal neck angulation superior to 60 degrees
4. Pre-op CT and post-operative/follow-up CT available
Exclusion Criteria
2. Non-injected or poorly injected pre-operative CT-scan precluding technical feasibility of the aortic digital twin
3. Absence of post-operative or follow-up CT-scan
4. Patient refusal of his personal information/medical data to be used in the context of the study
ALL
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Hôpital Louis Pradel
Bron, , France
Countries
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Other Identifiers
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69HCL24_0514
Identifier Type: -
Identifier Source: org_study_id
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