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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05041725
Other study ID # 20210000-2
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date November 1, 2021
Est. completion date December 31, 2022

Study information

Verified date September 2021
Source Konkuk University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study analyzes the impact of intraoperative Remimazolam infusion for postoperative sedation on the left ventricular global longitude strain (LV-GLS) patients undergoing cardiac surgery


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 15
Est. completion date December 31, 2022
Est. primary completion date November 30, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - elective off-pump coronary artery bypass surgery Exclusion Criteria: - arrhythmia - LV ejection fraction < 50 % - preoperative inotropic support

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Remimazolam Injection [Byfavo]
Remimazolam injection and continuous infusion for postoperative sedation, 0.2 mg/kg for 1 min and continuous infusion of 1-2 mg/kg/hour

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 change of the left ventricular global longitudinal strain mean values of the left ventricular global longitudinal strain after 3 minutes, 5 minutes and 10 minutes after the Remimazolam administration 1 minutes
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