(CVENT-PAI): Assessment of Plaque Vulnerability Using a Novel Technique: Multi-spectral PhotoAcoustic Imaging.

Sponsor
Centre Hospitalier St Anne (Other)
Overall Status
Terminated
CT.gov ID
NCT04763603
Collaborator
(none)
25
1
13.6
1.8

Study Details

Study Description

Brief Summary

Identification of intraplaque haemorrhage using MRI is technically demanding and sometimes uncomfortable. Photoacoustic imaging is a new non-invasive technique combining multi-wavelength infrared laser light and ultrasound imaging, able to discriminate blood and other components in the tissues. The measurement by the multi-spectral photoacoustic imaging is likely to be more acceptable and therefore could replace MRI.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    A total of 60 patients with stenosis grade of > 70% and considered for endarterectomy will be recruited for additional imaging. Pre-operative PA/US and 3D MR imaging will be conducted. Two patient groups are designed to allow performance assessment with respect to anatomy, i.e., penetration depth; One with favourable anatomy (i.e. superficial carotids, proximal plaques and low bifurcation), the other with no anatomical considerations. For in-vivo verification of the morphology and mechanical properties obtained with PA/US imaging, the pre-operative data will be compared to the MR data (imaging-imaging verification). Since the patient is operated on, endarterectomy specimens are available for histo-pathological examination and in-vitro testing for verification purposes: the excised tissue will be (snap freeze with liquid Nitrogen) transported to TUE in Eindhoven for in-vitro validation (imaging-histology verification). Paris patients will undergo surgery and tissues will be transferred to Eindhoven for in vitro mechanical testing. Because of the transfer (-80 °C), the rate of success for in vitro testing is expected to be smaller, around 40% (i.e. 12 subjects). Nevertheless, the power of the global analysis will be increased.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    25 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Assessment of Plaque Vulnerability Using a Novel Technique: Multi-spectral PhotoAcoustic Imaging.
    Actual Study Start Date :
    Jan 29, 2019
    Actual Primary Completion Date :
    Mar 17, 2020
    Actual Study Completion Date :
    Mar 17, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Evaluation of the device [18 month]

      The primary outcome is to evaluate the ability of the experimental device to visualize hemorrhage within the plaque. The primary endpoint will therefore be concordance with histology and plaque analysis (ex-vivo reference method) and MRI (invivo reference method).

    Secondary Outcome Measures

    1. Evaluation of anatomical concordance [18 month]

      The secondary objective of the study is to evaluate the concordance according to the anatomical characteristics of the patient. However, only patients without unfavorable anatomy will be included in the study.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Presence of at least one carotid plaque with a degree of stenosis 70% (NASCET), indication to surgery (endarterectomy),

    • Patients with favourable anatomy criteria :

    x Cranio-caudal length of normal or long neck x Cervical adiposity weak or absent x Carotid bifurcation in usual situation (at the level of the mandibular angle or lower) x Normal genicity of subcutaneous tissues x Calcification of arterial moderate or absent

    • Patients affiliated to the social health security system.
    Exclusion Criteria:
    • Refusal to participate,

    • any concomitant chronic condition hampering the realization of ultrasound scanner or MRI (allergy to gel, intolerance or contraindication to gadolinium).

    • Unstable patients with plaque claudication inducing procedure acceleration.

    • Patients with unfavourable anatomy criteria :

    x Cranio-caudal length of the neck very short x Significant cervical adiposity x Carotid bifurcation higher than the mandibular angle x High echogenic subcutaneous tissue x Calcification marked arterialH2020-ICT-29-2016 no. 731771 Ethics requirements x Patients with fat necks, Presence of extensive calcifications at the site of the stenosis.

    • Patients unable to consent.

    • Pregnant woman or breastfeeding woman

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sainte-Anne Hospital Paris Ile De France France 75014

    Sponsors and Collaborators

    • Centre Hospitalier St Anne

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Centre Hospitalier St Anne
    ClinicalTrials.gov Identifier:
    NCT04763603
    Other Study ID Numbers:
    • D18-P007
    First Posted:
    Feb 21, 2021
    Last Update Posted:
    Feb 21, 2021
    Last Verified:
    Feb 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Centre Hospitalier St Anne

    Study Results

    No Results Posted as of Feb 21, 2021