Clinical Trials Directory

Trials / Completed

CompletedNCT05820828

Comparing Air Embolic Load in Two Venous Cannulation Methods, 40 Patients Undergoing Elective Valve Surgery.

Does Venous Cannulation Method Affect Air Embolic Load to the Patient During Extracorporeal Circulation?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Petronella Torild · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this single center prospective controlled observational and interventional trial is to investigate and compare origin of air emboli when different venous cannulation methods is used in patients undergoing cardiac surgery with extracorporeal circulation. 40 consecutive elective patients will be included in two groups, depending on the procedure requiring bicaval or cavoatrial cannulation. After assorted into respective group, patients will be block randomized (five groups consisting of eight patients each) to either intervention group (low venous reservoir volume, 200-300 mL) or control group (venous reservoir volume \> 300 mL). Primary endpoint is to investigate if the amount of air emboli passing through the oxygenator to the arterial line differs between bicaval and cavoatrial venous cannulation during extracorporeal circulation. Secondary endpoints are the relative difference in amount air emboli between the groups, if there is any correlation between the amount of air in venous line and the amount of air passing through the oxygenator to the arterial line during extracorporeal circulation, and if difference is seen on the amount of air passing through the oxygenator depending on the level of volume in the venous reservoir.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTVolume controlVolume control in venous reservoir during extracorporeal circulation.

Timeline

Start date
2023-04-21
Primary completion
2023-08-28
Completion
2023-08-28
First posted
2023-04-20
Last updated
2024-04-03

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT05820828. Inclusion in this directory is not an endorsement.