Ignite Creation Date:
2024-06-16 @ 11:48 AM
Last Modification Date:
2024-10-26 @ 3:30 PM
Study NCT ID:
NCT06428877
Status:
COMPLETED
Last Update Posted:
2024-05-24
First Post:
2024-05-16
Brief Title:
Monocentric Retrospective Observational Study Analysis of Gore Excluder ACS Device Using Numerical Simulation
Sponsor:
Hospices Civils de Lyon
Organization:
Hospices Civils de Lyon
Study Overview
Official Title:
Monocentric Retrospective Observational Study Analysis of Gore Excluder ACS Device Using Numerical Simulation
Status:
COMPLETED
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
ACSSim
Brief Summary:
andated when the risk of rupture is low and interventional treatment is offered to patients at high risk of rupture Rupture risk is driven by aneurysm diameter and growth rate Aneurysms with diameter greater than 55 mm andor growth rate greater than 1 cm per year are at high risk of rupture Open surgery and endovascular treatment are the two types of interventions Open repair consists in replacing the aneurysmal part of the aorta using a synthetic fabric prosthesis after the abdomen has been opened and the aorta clamped This invasive procedure is associated with a 3-10 post-operative mortality Endovascular repair EVAR consists in excluding the aneurysm sac by inserting a self-expanding prosthesis called stent-graft through very small groin incisions without abdominal opening nor aortic clamping This minimally invasive procedure is associated with a significantly reduced post-operative mortality around 1 However hostile proximal neck anatomy including high angulation is associated with higher rates of type IA endoleak reintervention and long-term mortality For this reason a conformable design of the Excluder stent-graft has been engineered with initial satisfactory results in patients with highly angulated or short necks However these satisfactory results have been obtained in carefully selected patients from experienced centers and a tool demonstrating adequate apposition of the Gore ACS is lacking Study Device Description Numerical simulation has been used successfully to predict stent-graft behavior during FEVAR Preliminary studies have also demonstrated to applicability of the technology to standard infrarenal devices including in the setting of very tortuous anatomies9 The potential of numerical simulation to predict stent-graft apposition of Gore ACS in highly angulated necks appears very promising to enhance patient selection
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None