Examining blood flow changes in the aorta after endovascular treatment for aortic dissection
Radiological Study of the Hemodynamic Changes in the Aorta and Its Branches Before and After Endovascular Treatment of the Aortic Dissection
This study is testing how blood flow in the aorta changes after a special treatment for aortic dissection to see if it helps patients feel better and avoid complications.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 6 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Hospices Civils de Lyon Academic / other |
| Locations | 1 site (Bron) |
| Trial ID | NCT03669055 on ClinicalTrials.gov |
What this trial studies
This study investigates the hemodynamic changes in the aorta following endovascular treatment for aortic dissection, a serious condition affecting the aorta. Patients requiring this treatment will undergo magnetic resonance imaging (MRI) to evaluate the dynamic changes in the aorta post-procedure. The study aims to assess the effectiveness of the endoprosthesis in improving blood flow and reducing complications associated with aortic dissection. By utilizing advanced imaging techniques, the research seeks to provide insights into the outcomes of endovascular interventions.
Who should consider this trial
Good fit: Ideal candidates include patients diagnosed with aortic dissection who require endovascular treatment as determined by a multidisciplinary team.
Not a fit: Patients needing emergency interventions or those with contraindications to endovascular treatment or MRI will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies and outcomes for patients with aortic dissection.
How similar studies have performed: Other studies have shown promise in using advanced imaging techniques for evaluating aortic conditions, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Bron
- Hopital Louis Pradel — Bron, France (Recruiting)
Study contacts
- Study coordinator: Benoit Cosset, MD
- Email: benoit.cosset@chu-lyon.fr
- Phone: 472115170
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.