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The purpose of this research is to determine the feasibility of a larger, future study proposing a multimodal approach using cardiac CT and MRI to assess the risk of developing left ventricular (LV) systolic dysfunction in patients with mitral regurgitation (MR).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Chronic severe primary mitral regurgitation | Adults with chronic severe primary mitral regurgitation undergoing robotic mitral annuloplasty at Mayo Clinic Rochester |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cardiac MRI | Diagnostic Test | Each subject will receive two cardiac MRI scans (with and without contrast), one preoperative and another 6-12 months after. The duration of each MRI is approximately 45-60 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Recruitment Rate | Number of subjects consented to participate in study | 2 years |
| Dropout Rate | Number of subjects to withdraw from study | 2 years |
| Systolic Dysfunction | Number of subjects to experience postoperative systolic dysfunction, defined as Left ventricular ejection fraction (LVEF) < 50% | 2 years |
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Inclusion Criteria:
Exclusion Criteria:
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Adults with chronic severe primary mitral regurgitation undergoing robotic mitral annuloplasty at Mayo Clinic Rochester
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Cardiovascular Surgical Research | Contact | (507) 266-7982 | cvsurgresearch@mayo.edu |
| Name | Affiliation | Role |
|---|---|---|
| Arman Arghami, MD, MPH | Mayo Clinic | Principal Investigator |
| Alex Bratt, MD | Mayo Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic | Recruiting | Rochester | Minnesota | 55905 | United States |
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| ID | Term |
|---|---|
| D018487 | Ventricular Dysfunction, Left |
| ID | Term |
|---|---|
| D018754 | Ventricular Dysfunction |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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