Can a novel perfusion monitor help us defining optimal flow for patients on cardiopulmonary bypass.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON28731

Enrollment

150

Registered

2014-04-23

Start date

2014-02-17

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

Cardiopulmonary bypass, perfusion monitor, cardiovascular patients, adequate oxygen delivery, hypo-perfusion, hyper perfusion, postoperative complications, individual circulatory treatment.

Interventions

Arterial and venous connector for inline measurement. Regular blood gas analysis. Blood flow sensor measurement.

Eligibility

Inclusion criteria

Inclusion criteria: -Patients scheduled for cardiac surgery. -Normothermic cases and maximum duration less than 2 hours.

Exclusion criteria

Exclusion criteria: -Complicated cases -CPB duration over 2 hours -renal insufficiency -emergency -reanimation -salvage and existing inflammatory conditions.

Design outcomes

Primary

Measure	Time frame
Which oxygen flow gives hyperlactatemia?	—

Secondary

Measure	Time frame
Evaluation of kidney function.	—

Contacts

Public ContactVeerle Mossevelde, van

Laarbeeklaan 101

veerle.vanmossevelde@uzbrussel.be+32 (0)2 4763134

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)