In vivo study of pulse conductance of oxygenators during pulsatile flow

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON20861

Enrollment

Registered

2008-06-17

Start date

2008-07-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

oxgenator pulsatile flow heart-lung machine

Interventions

Non-interventional study, therefore non-applicable

Eligibility

Inclusion criteria

Inclusion criteria: 1. 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. 2. Calculated bypass flow of 5 l/min. 3. Written informed consent. 4. Age of 18 and older.

Exclusion criteria

Exclusion criteria: 1. All other patients that do not comply with the inclusion criteria given above, e.g. patients receiving valve surgery, or combined CABG / valve surgery. 2. No written informed consent.

Design outcomes

Primary

Measure	Time frame
To measure pulse conductance of two standard types of oxygenators standard used during coronary artery bypass surgery using a standard heart-lung machine.	—

Secondary

Measure	Time frame
To measure/record the standard normalized index of haemolysis during elective coronary artery bypass surgery using a standard heart-lung machine.	—

Contacts

Public ContactAntoine P. Simons

University Hospital Maastricht Dept. Cardiothoracic Surgery P.O. box 5800

antoinepsimons@ctc.unimaas.nl+31 (0)43 3881066

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)