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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03183414
Other study ID # nWMO 220
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 6, 2017
Est. completion date June 30, 2018

Study information

Verified date November 2019
Source Medical Centre Leeuwarden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date June 30, 2018
Est. primary completion date June 20, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Other:
echocardiographic measurements
echocardiographic parameters of the RV, measured with TEE and the right ventricular ejection fraction (thermodilution)

Locations

Country Name City State
Netherlands Medical Centre Leeuwarden Leeuwarden

Sponsors (1)

Lead Sponsor Collaborator
Medical Centre Leeuwarden

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary The correlation between echocardiographic parameters of the RV, measured with TEE and the RVEF measured with the pulmonary artery catheter The correlation between echocardiographic parameters of the RV, measured with TEE and the RVEF measured with the pulmonary artery catheter. during cardiac surgery
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