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Simulation of Stent-graft Deployment in Aortic Arch Aneurysms

C

Centre Hospitalier Universitaire de Saint Etienne

Status

Completed

Conditions

Aortic Arch Aneurysm

Treatments

Other: Collection of datas

Study type

Observational

Funder types

Other

Identifiers

NCT04244188
IRBN032019/CHUSTE

Details and patient eligibility

About

Total endovascular repair of the aortic arch represents a promising option for patients ineligible to open surgery. Custom-made design of stent-grafts (SG), such as the Terumo Aortic® RelayBranch device (DB), requires complex preoperative measures. Accurate SG deployment is required to avoid intraoperative or postoperative complications, which is extremely challenging in the aortic arch. In that context, the investigators aim is to develop a computational tool able to predict SG deployment in such highly complex situations. Four patient-specific cases will be performed with complete deployment of the DB and its bridging stents in aneurysmal aortic arch. Deviations of simulation predictions from actual stent positions will be estimated based on post-operative scan and a sensitivity analysis will be performed to assess the effects of material parameters. If good agreement between simulation and reality is obtained, numerical simulations will show their ability to successfully predict the DB deployment in complex anatomy. The results will emphasize the potential of computational simulations to assist practitioners in planning and performing complex and secure interventions.

Full description

The process of numerical simulation of double-branched device in aortic arch aneurysm involves: (i) aortic arch segmentation with data from the preoperative CT-scan (ii) numerical modeling of the actual stentgraft used to treat the patient (iii) simulation of stentgraft deployment in aortic arch (iv) validation of simulation results based on post-operative CT scan images The goal of this study is to develop a numerical model of stentgraft deployment able to predict the actual deployement of the double branched device in aortic arch aneurysm.

Enrollment

4 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aortic arch aneurysms suitable for treatment using double-branched device Bolton

Exclusion criteria

  • Failure to generate an adequate FE model of patient arteries (no preoperative multidetector contrast-enhanced CT-scan available, preoperative CT-scan slice thickness greater than 1mm, preoperative CT- scan with artifacts)
  • dissected aneurysm

Trial design

4 participants in 1 patient group

Patients treated for aortic arch aneurysms
Description:
Patients treated for aortic arch aneurysms by double branched endovascular repair (Bolton Medical) will be included.
Treatment:
Other: Collection of datas

Trial contacts and locations

2

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Central trial contact

Iness AYARI, CRA; Jean-Noël ALBERTINI, PhD

Data sourced from clinicaltrials.gov

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