Clinical Trials Directory

Trials / Completed

CompletedNCT03717649

Negative Venous Line Pressure in a Miniaturised Cardiopulmonary Bypass Circuit (CPB)

Negative Venous Line Pressure in a Miniaturised Cardiopulmonary Bypass Circuit - the Influence of a Fenestrated Venous Cannula and Its Effect on Pump Flow

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
48 (actual)
Sponsor
University Hospital Plymouth NHS Trust · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Study to measure the ability of a 'fenestrated' venous line cannula to reduce the negative line pressure seen with kinetic-assist active venous drainage (KAVD) in a standard miniaturised cardiopulmonary bypass circuit and thereby increase the flow characteristics of the bypass pump.

Detailed description

To investigate whether a new venous drainage pipe (cannula) which has three sets of drainage holes (three-stage) compared with the standard two-stage cannula, or a three-stage which also has additional windows (fenestrations), can improve the drainage of blood into the circuit, reducing the negative pressure produced and increase the blood flow delivered to the patient. Patients who consent to participate will be randomly assigned to one of three types of venous cannula: 1. Standard venous cannulation with a two-stage venous cannula 2. The three-stage cannula (91437C, Medtronic) 3. The fenestrated three-stage cannula (MC2X, Medtronic)

Conditions

Interventions

TypeNameDescription
DEVICEConventional 2-stage venous cannulavenous cannula
DEVICEConventional 3-stage venous cannulavenous cannula
DEVICEFenestrated 3-stage venous cannulavenous cannula

Timeline

Start date
2016-01-12
Primary completion
2016-10-31
Completion
2016-10-31
First posted
2018-10-24
Last updated
2018-10-24

Source: ClinicalTrials.gov record NCT03717649. Inclusion in this directory is not an endorsement.