4DAo: Hemodynamic Changes in the Aorta After Endovascular Treatment of the Aortic Dissection

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Recruiting
CT.gov ID
NCT03669055
Collaborator
(none)
6
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Study Details

Study Description

Brief Summary

Aortic dissection (AD) is a serious pathology affecting one person for 300 000 habitants per year. In case of complicated AD on the descending aorta, it is necessary to perform an endovascular surgery in association with medical treatment. An endoprosthesis is implanted on the descending thoracic aorta in order to close the main intimal tear. This closure lead to an increase in the thoracic true lumen diameter, a decrease in the thoracic false lumen diameter, a better perfusion of the aortic branches. Furthermore, even in case of open surgical treatment of the ascending aorta it can be necessary to perform an endovascular treatment on the descending aorta, either to prevent and treat aneurysmal evolution or to treat patent malperfusion syndrome.

CT and Magnetic Resonance angiography, by the realization of an aortic morphologic evaluation, are the two key imaging exams in the DA. Nevertheless, CT can't provide aortic dynamic evaluation, contrary to MRI. This exam, thanks to the phase-contrast sequence can measure velocity and flow data in vessels, including aorta but also true and false lumen in the AD. Thus, by verifying the perfusion of the aortic true lumen and the aortic branches it is possible to perform an early evaluation of the endovascular treatment of the DA.

Actually, only one study has realized an aortic dynamic evaluation on the AD, unfortunately this study was limited to non-operated patients.

In order to assess the place of MRI in the AD, the ingestigation propose to determine if phase-contrast MRI is able to evaluate the impact of the endovascular treatment on the hemodynamic state of the aorta and its branches.

Condition or Disease Intervention/Treatment Phase
  • Other: Magnetic Resonance Imaging
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
6 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Radiological Study of the Hemodynamic Changes in the Aorta and Its Branches Before and After Endovascular Treatment of the Aortic Dissection
Actual Study Start Date :
Mar 7, 2019
Anticipated Primary Completion Date :
Dec 7, 2021
Anticipated Study Completion Date :
Dec 7, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pre-operative and post operative Magnetic Resonance Imaging

Realization of an angio-MRI with 4D phase contrast sequence before and after the endovascular treatment of the aortic dissection

Other: Magnetic Resonance Imaging
Realization of a MRI before and after the endovascular treatment of the aortic dissection. Use of the 4D phase-contrast sequence during the MRI.

Outcome Measures

Primary Outcome Measures

  1. Comparative measurement of the flow in the aortic true lumen before and after endovascular treatment of the aortic dissection [change from day 0 and day 16]

    The flows are measured in ml/s at several locations of the aortic true lumen. The flows are measured during the two MRI and compared with each other.

Secondary Outcome Measures

  1. Comparative measurement of the flow in the aortic false lumen before and after endovascular treatment of the aortic dissection [change from day 0 and day 16]

    The flows are measured in ml/s at several locations of the aortic false lumen. The flows are measured during the two MRI and compared with each other.

  2. Comparative measurement of the flow in the aortic branches before and after endovascular treatment of the aortic dissection [day 0 and day 16]

    The flows are measured in ml/s in the celiac artery, the superior mesenteric artery, the inferior mesenteric artery, the right and left renal artery, the right and left primitive iliac artery. The flows are measured during the two MRI and compared with each other.

  3. Comparative measurement of the number of intimal tear identified through 4D phase-contrast MRI relative to the number of intimal tear identified through Angio MRI before endovascular treatment of the aortic dissection [change from day 0 and day 16]

    In the 4D phase-contrast MRI, an intimal tear is identified by a streamline going from the true lumen to the false lumen. In the Angio MRI, an intimal tear is identified by the visualization of the passage of the contrast agent from the true lumen to the false lumen.

  4. Flow measurement through intimal tear with 4 Dimensions (4D) phase-contrast MRI before and after endovascular treatment of the aortic dissection [change from day 0 and day 16]

    The intimal tears are identified thanks to the Angio MRI. The flows are measured during the two MRI and compared with each other.

  5. Comparative measurement through 4D phase-contrast MRI of the shear forces before and after endovascular treatment of the aortic dissection [change from day 0 and day 16]

    Shear forces are measured thanks to the 4D phase contrast MRI.

  6. Comparative measurement through 4D phase-contrast MRI of parietal energy before and after endovascular treatment of the aortic dissection [change from day 0 and day 16]

    Parietal energy is measured thanks to the 4D phase contrast MRI.

  7. Comparative measurement through 4D phase-contrast MRI of the presence of helicoidal flow before and after endovascular treatment of the aortic dissection [change from day 0 and day 16]

    The presence of a perpendicular flow to the main aortic flow is identified thanks to the 4D phase contrast MRI. The helicoidal flow is quantified by the degree of rotation between the beginning of the end of the cardiac cycle in millisecond.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with an aortic dissection requiring endovascular treatment

  • The endovascular treatment will be indicated according to the guidelines after medical, radiological and surgical multidisciplinary discussion in our hospital.

  • Patients that have signed the informed consent form.

  • Members of a social protection scheme.

Exclusion Criteria:
  • Patients with an aortic dissection requiring an emergency intervention

  • Patients with a contra-indication to endovascular treatment

  • Contra-indication to MRI: claustrophobia, ferromagnetic materials: pacemaker, prosthetic heart valve, implantable cardioverter defibrillators, vascular clip

  • Pregnancy

  • Breastfeeding

  • Dementia

  • Patients under guardianship

  • Patients with difficulty in understanding the French language

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hopital Louis Pradel Bron France

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT03669055
Other Study ID Numbers:
  • 69HCL18_0361
  • 2018-A01742-53
First Posted:
Sep 13, 2018
Last Update Posted:
Dec 7, 2020
Last Verified:
Dec 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hospices Civils de Lyon
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 7, 2020