In vivo study of pulse conductance of oxygenators during pulsatile flow

In vivo study of pulse conductance of oxygenators during pulsatile flow - Pulse conductance of oxygenators

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON32106

Enrollment

Registered

2008-06-04

Start date

2008-06-23

Completion date

Unknown

Last updated

2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coronary surgery open-heart surgery

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Patients scheduled for elective CABG using a standard heart-lung machine with either a standard used Maquet Quadrox HMO 2000 oxygenator, or a standard clinically equivalent Terumo Capiox SX18 oxygenator, using standard pulsatile perfusion at the University Hospital Maastricht. -Written informed consent.

Exclusion criteria

Exclusion criteria: -All other patients that do not comply with the inclusion criteria given above, e.g. patients receiving valve surgery, or combined CABG and valve surgery. -No written informed consent.

Design outcomes

Primary

Measure	Time frame
Puls conductance of the oxygenators Maquet Quadrox HMO 2000 and Terumo Capiox SX18 during pulsatile perfusion with a heart-lung machine.	—

Secondary

Measure	Time frame
Blood damage, measured on the basis of standard measured/determined normalized index of hemolysis during pulsatile perfusion with a heart-lung machine.	—

Countries

Netherlands

Outcome results