Multi-Center Observational study to assess optimal ECMO settings during the first hours of Extra-Corporeal Cardiopulmonary Resuscitation.

Multi-Center Observational study to assess optimal ECMO settings during the first hours of Extra-Corporeal Cardiopulmonary Resuscitation. - Observational study to assess optimal ECPR settings after resuscitation

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON50088

Enrollment

Registered

2019-11-01

Start date

2019-01-04

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

Cardiac arrest Reperfusion injury after extracorporeal cardiopulmonary resuscitation

Interventions

Cardio-Pulmonary resuscitation

Extra-Corporeal CardioPulmonary Resuscitation

ischemia-reperfusion injury

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Witnessed cardiac arrest or signs of life during CPR (such as gasping or movement) - Age>18 and 10 mmHg) provided for a minimum of 15 minutes without ROSC - Cerebral oxymetry monitoring initiated during CPR preceding ECPR

Exclusion criteria

Exclusion criteria: - Patients with a GCS

Design outcomes

Primary

Measure	Time frame
CPC* 2 at hospital discharge	—

Secondary

Measure	Time frame
- CPC1 2, 6 months after arrest - GCS>13 at day 28 - GCS > 13 at any time - 28 days Mortality - Hospital survival	—

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)