Clinical Trials Directory

Trials / Completed

CompletedNCT06784570

Impact of Perioperative Levosimendan on Patients Undergoing Cardiac Surgery With Low Ejection Fraction

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
240 (actual)
Sponsor
Zagazig University · Other Government
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

to compar levosemindan to other cardiac intropic medications that strengthen the heart in diffrent common adult heart surgery with patients with low ejection fraction(weak heart)

Detailed description

in this study show the effect of levosemindan use during coronary artery surgery ,heart valve surgery and combined coronary and valve surgery in comparison to other traditional medications with patients with low ejection fraction(weak heart)

Conditions

Interventions

TypeNameDescription
DRUGlevosemindanIn common practice the loading dose is omitted as it is associated with hypotension.9 Usual dose range: 0.05 to 0.2 microg/kg/min. Dose based on actual body weight up to a maximum of 120 kg.5 Commence infusion at 0.05 microg/kg/min. If the initial rate is tolerated, consider increasing the maintenance rate to 0.1 microg/kg/min after 60 minutes. If the patient remains haemodynamically stable, further increase the dose to 0.2 microg/kg/min for the remainder of the infusion.
DRUGadrenaline,noreadrenaline,dopamine and doputamineadrenaline:\*4 9 %$ 0 \*\*\*\*8\*4\* 9 : ,- 4 - \*4 9 \* C % F\*4 9 9 9 noreadrenaline:# \*4 9 C % 9 F 9 9 \*4\* Q\*4 9 9 dopamine:9 \* C % 9 F 9 9 ) \* 9 9 dobutamine:9 \* C % F 9 9 9 \* 9 9

Timeline

Start date
2021-01-01
Primary completion
2024-03-01
Completion
2024-08-01
First posted
2025-01-20
Last updated
2025-01-20

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06784570. Inclusion in this directory is not an endorsement.