MRI as a Predictor of Outcomes in Patients Undergoing Mitral Valve Surgery
NCT ID: NCT03012178
Last Updated: 2018-01-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2017-01-31
2020-12-31
Brief Summary
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Detailed Description
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The most common diagnostic tool to assess the severity of MR is echocardiography. Several studies have shown that echocardiography parameters used to quantify and qualify MR have high inter-observer and intra-observer variability, calling the accuracy of these parameters into question. Furthermore, studies have shown that there is a significant degree of discordance between echocardiography and MRI when assessing MR, particularly among patients referred for mitral valve surgery. In a recent study, quantification of mitral regurgitant volume MRI was found to be more accurate than echocardiography in patients who underwent mitral valve surgery. All 38 patients who underwent mitral valve surgery in this study were deemed appropriate according the ACC/AHA guidelines based on echocardiographic findings. However, more than 2/3rds of patients who underwent mitral valve surgery in this study did not have severe MR by MRI. Thus, we propose this prospective multicenter trial to assess: 1) the severity of MR by MRI in patients undergoing mitral valve surgery. 2) the impact of mitral valve surgery on quality of life and healthcare costs in the context of MR severity by MRI, 3) assess patient outcomes post surgery in the context of MR severity by MRI and 4) the likelihood of valve replacement vs. repair according to MR severity by MRI.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Mitral Valve Surgery
Patients undergoing ACC/AHA guideline directed mitral valve surgery for mitral insufficiency.
Mitral valve surgery
ACC/AHA guideline directed mitral valve repair or replacement
Interventions
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Mitral valve surgery
ACC/AHA guideline directed mitral valve repair or replacement
Eligibility Criteria
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Inclusion Criteria
* Able to give informed consent.
* Undergoing lone mitral valve surgery for chronic primary mitral regurgitation within 30 days.
* Indication for mitral valve surgery is a class I or IIa according to the 2014 ACC/AHA guidelines for the management of valvular heart disease.
Exclusion Criteria
* Have a device which is not compatible with MRI
* Claustrophobia preventing MRI.
* Concomitant CABG, other valve surgery, or other cardiac surgery.
* Atrial fibrillation or other substantial arrhythmia that would substantially degrade MRI image acquisition.
18 Years
ALL
No
Sponsors
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Atlantic Health System
OTHER
Responsible Party
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Locations
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Morristown Medical Center
Morristown, New Jersey, United States
Countries
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Central Contacts
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Facility Contacts
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References
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Uretsky S, Gillam LD, Biederman RWW, Han Y, Jacob R, Martin ET, Langer M, Choi AD, Sultan I, Cavalcante JL, Shah DJ, Tong MS, Wolff SD, Sakul S, Guglielmo M, Pontone G. Sex differences in pre- and post-surgical left ventricular remodelling and outcomes in primary mitral regurgitation. Eur Heart J Cardiovasc Imaging. 2025 Jul 31;26(8):1429-1437. doi: 10.1093/ehjci/jeaf151.
Other Identifiers
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967510-2
Identifier Type: -
Identifier Source: org_study_id
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