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Clinical Trials/NCT03183414
NCT03183414CompletedNot Applicable

Right Ventricular Dysfunction in Cardiac Surgery

Medical Centre Leeuwarden1 site in 1 country15 target enrollmentStarted: September 6, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
15
Locations
1
Primary Endpoint
The correlation between echocardiographic parameters of the RV, measured with TEE and the RVEF measured with the pulmonary artery catheter

Study Overview

Brief Summary

To establish the correlation between echocardiographic parameters of the RV, measured with TEE and the right ventricular ejection fraction (thermodilution). To identify a time in the perioperative process when RV dysfunction occurs.

Detailed Description

Measurements with echocardiography were done during cardiac surgery to observe the right ventricular dysfunction in the perioperative process

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • cardiac surgery patients
  • elective, isolated aortic valve replacement or coronary artery bypass grafting in combination with aortic valve replacement

Exclusion Criteria

  • age < 18

Outcomes

Primary Outcomes

The correlation between echocardiographic parameters of the RV, measured with TEE and the RVEF measured with the pulmonary artery catheter

Time Frame: during cardiac surgery

The correlation between echocardiographic parameters of the RV, measured with TEE and the RVEF measured with the pulmonary artery catheter.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Medical Centre Leeuwarden
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Matty Koopmans

MSc

Medical Centre Leeuwarden

Study Sites (1)

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