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Interest of Pre-operative Use of 3D Printing for Endovascular Treatment of Unruptured Intracranial Aneurysms With Intrasaccular Flow Disruptor

Not Applicable
Not yet recruiting
Conditions
Intracranial Aneurysm
Interventions
Procedure: 3D anatomical model of aneurysm
Registration Number
NCT05665309
Lead Sponsor
Centre Hospitalier Universitaire de Besancon
Brief Summary

This is a preliminary randomised controlled trial comparing the use of pre-operative 3D models to select an intrasaccular flow disruptor for endovascular aneurysm cure.

Detailed Description

Patients will be randomised 3:1 either in the intervention or control group. Intervention consists of using the pre-operative Digital Subtraction Angiography (DSA) to create a 3D plastic model. This model is used to test different sizes of device. At the end of this pre-operative test a single device is recommended for the real procedure. The control group will use the current method for size selection (measurement of mean width and minimum height) on DSA.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Intracranial aneurysm, suitable for a treatment by Woven Endobridge (WEB) device after multidisciplinary team decision
  • Consent form signed
  • The patient benefits from health insurance
Exclusion Criteria
  • Legal incapacity
  • Women at risk of pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
With 3D anatomical model3D anatomical model of aneurysmSurgery prepared using 3D anatomical model of the aneurysm
Primary Outcome Measures
NameTimeMethod
Proportion of patients with successful procedureDay 0

Proportion of patients for which flow disruption succeeded at first intent, without any change of size required for WEB disruptor

Secondary Outcome Measures
NameTimeMethod
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