Right Ventricular Dysfunction in Cardiac Surgery Patients
NCT ID: NCT03183414
Last Updated: 2019-11-26
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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COMPLETED
15 participants
OBSERVATIONAL
2017-09-06
2018-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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cardiac surgery patients
cardiac surgery patients with a significant peroperative aortic valve stenosis (gradient\>40mmHg and/or aortic valve area \<1cm2). During cardiac surgery measurements of right ventricular dysfunction were taken by echocardiography
echocardiographic measurements
echocardiographic parameters of the RV, measured with TEE and the right ventricular ejection fraction (thermodilution)
Interventions
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echocardiographic measurements
echocardiographic parameters of the RV, measured with TEE and the right ventricular ejection fraction (thermodilution)
Eligibility Criteria
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Inclusion Criteria
* elective, isolated aortic valve replacement or coronary artery bypass grafting in combination with aortic valve replacement
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Frisius Medisch Centrum
OTHER
Responsible Party
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Matty Koopmans
MSc
Principal Investigators
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Christiaan Boerma, MD
Role: PRINCIPAL_INVESTIGATOR
MCL
Locations
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Medical Centre Leeuwarden
Leeuwarden, , Netherlands
Countries
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Other Identifiers
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nWMO 220
Identifier Type: -
Identifier Source: org_study_id
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