Exercise Physiology in Patients With Aortic Aneurysm and Its Correlation With Mechanical Properties of Aortic Tissue

NeuroTherapia, Inc.

Status: Enrolling

Conditions: Aortic Aneurysm

Treatments: Diagnostic Test: Exercise MRI

Study type: Interventional

Funder types: Other

Identifiers

NCT06789809

20-310

Details and patient eligibility

About

Aortic aneurysm patients benefit from exercise yet patients and physicians do not know a safe level. Cardiac MRI (CMR) is the most comprehensive imaging modality for phenotypic evaluation of patients with cardiac disease but it has not been used to study aneurysm patients. The purpose of this project is use exercise CMR to understand regional aortic function and quantify aortic elasticity in these populations while exercising. This project will correlate the exercise CMR data with the biomechanical properties of the patient's aortic tissue, including epiaortic ultrasound and TEE performed during aortic repair, and explanted aortic specimens subjected to ex vivo uniaxial tensile testing. Correlating this data with aortic response to exercise will allow us to understand how aortic size, in vivo circumferential strain values, ex vivo aortic efficiency and mechanical failure all relate to exercise physiology.

Full description

Engaging in regular exercise in controls lowers blood pressure over time, and this is associated with a lower risk of future aortic complications. However, it is not known what level of exercise is safe for aneurysm patients.

Cardiac MRI (CMR) is the most comprehensive imaging modality for phenotypic evaluation of patients with cardiac disease. It has been limited in its use because exercise stress MRI is not widely available due to the need for MRI safe exercise equipment. However, the Cleveland Clinic has purchased a Lode MRI compatible exercise ergometer that is FDA approved and compatible with our 3T cardiac MRI scanner.

By conducting a study using this imaging modality we will be able to observe aortic blood flow, specifically compliance, distensibility, maximum rates of systolic distension and diastolic recoil, at different locations along the ascending and descending aorta, as well as aortic pulse wave velocity. A more comprehensive analysis of these variables will be critical to understanding how the aorta responds during times of stress in aneurysm patients.

Enrollment: 35 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Healthy controls for baseline comparison

   1. Must be 18 years or older
   2. No history of cardiovascular disease, neither hypertension, diabetes nor hypercholesterolemia

2. Aneurysm patients who have not yet been operated on but are currently being monitored

   1. Must be 18 years or older
   2. No history of operation for aortic aneurysm

3. Pre-operative aneurysm patients: imaged pre-operatively and 12 months

   1. Patients admitted at the CCF cardiothoracic services for elective surgery due to aortic aneurysms
   2. Must be 18 years or older

Exclusion criteria

For all patients:

• Contra-indication for MRI

  • Heart pacemaker/defibrillator.
  • Electronic/implanted stimulators or devices, including deep brain stimulator, vagus nerve stimulator, bladder stimulator, spine stimulator, neurostimulators; implanted electrodes or wires.
  • Cochlear implant or other ear implants.
  • Implanted drug pumps (insulin, narcotic/pain medications, drugs to treat spasticity).
  • Programmable shunt.
  • Aneurysm clips and coils.
  • Stents (not located in heart).
  • Filters (for example, blood clot filters).
  • Metal fragment in your body or eye (eg, BBs, bullets, shrapnel, metal pieces or shavings).

• Congenital heart diseases such as patent ductus arteriosus, coarctation of aorta, ASD and VSD

• Presence of A-V fistula or intracardiac shunts

• Moderate or severe dysfunction in multiple valves

• Patients with significant claustrophobia

• Patients unable to pedal a supine bicycle

• Those who require supplemental oxygen

Specific Exclusion Criteria:

1. Healthy controls for baseline comparison

   1. Excluded if using cardioprotective medication
   2. Have a bicuspid aortic valve diagnosed using MRI

2. Pre-operative aneurysm patients: imaged pre-operatively and at 12 months a. Patients with traumatic aortic rupture

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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35 participants in 3 patient groups

Healthy Controls

Experimental group

Description:

Exercise MRI

Treatment:

Diagnostic Test: Exercise MRI

Aneurysm Being Monitored

Experimental group

Description:

Exercise MRI

Treatment:

Diagnostic Test: Exercise MRI

Pre-operative Aneurysm Patients

Experimental group

Description:

Exercise MRI

Treatment:

Diagnostic Test: Exercise MRI