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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04153383
Other study ID # KUH0000000123
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 2024
Est. completion date December 2024

Study information

Verified date September 2023
Source Konkuk University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to analyze the changes in cardiac performance before and after milrinone administration in order to find out whether milrinone improves LV performance in patients undergoing coronary artery bypass surgery.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - patient agree and provide written informed consent. - patient undergoing elective coronary artery bypass graft surgery - preoperative LV EF>50% (TTE) Exclusion Criteria: - preoperative cardiac dysrhythmia - preoperative IABP - use of other inotropic agents

Study Design


Intervention

Drug:
Milrinone Injection
giving IV milrinone: 50 mcg/kg loading dose by IV push over 10 minutes, then 0.375-0.75 mcg/kg/min IV

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Konkuk University Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary TMAD of ticuspid annulus during early relaxation 15 mini after milrinone administration
Secondary global longitudinal strain of the right ventricle 15 mini after milrinone administration
Secondary left ventricular ejection fraction 15 min after milline administration
Secondary global longitudinal strain of the left ventricle 15 min after milline administration
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