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Prospective Evaluation of the Biomechanical Properties of the Thoracic Aorta Coupling Magnetic Resonance Imaging and In-vitro Elasticity Tests in Patients With Ascending Aortic Aneurysm

Prospective Evaluation of the Biomechanical Properties of the Thoracic Aorta Coupling Magnetic Resonance Imaging and In-vitro Elasticity Tests in Patients With Ascending Aortic Aneurysm

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03746964
Acronym
MECATHOR
Enrollment
200
Registered
2018-11-20
Start date
2018-12-17
Completion date
2027-02-28
Last updated
2026-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patient With Ascending Aortic Aneurysm With Surgical Indication for Replacement

Brief summary

The biomechanical properties of the aorta are currently poorly understood. A better understanding would optimize surgical indications and monitoring techniques for patients with thoracic aortic aneurysms.

Interventions

PROCEDURECardiac MRI

Preoperative cardiac MRI

OTHERin-vitro elasticity tests

in-vitro elasticity tests performed on a segment of ascending aorta collected during surgery

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Person who has given oral consent * Patient with ascending aortic aneurysm with surgical indication for replacement * Age \> 18 years old * Scheduled surgery

Exclusion criteria

* Person not affiliated to the national health insurance system * Protected adult * Pregnant or breastfeeding woman * MRI Contraindication * Emergency surgical procedure

Design outcomes

Primary

MeasureTime frame
aortic compliance by cardiac MRIBefore surgery
In-vitro testing of the elasticity of the aortic wall fragment collected during surgery.through study completion, an average of 12 months

Countries

France

Contacts

Primary ContactComlan BLITTI
comlanmawuko.blitti@chu-dijon.fr+33 3 80 29 33 52

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026