Cerebral Oximetry, Pulmonary Artery Catheter Parameters and ECMO Flow in Patients Supported With Veno-arterial ECMO

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorAssiut University

About this trial

for patients connected to VA ECMO due to cardiogenic shock, monitoring:

1. Cerebral Oximetry 2. ECMO Parameters ECMO blood flow (L/min) every 12 hours. Sweep gas flow Cannulation configuration 3. Pulmonary Artery Catheter Data and hemodynamics:

Cardiac output / cardiac index, SvO₂, Central venous pressure (CVP). 4. other variables: P/F ratio, MAP, Heart rate, Arterial blood gases, hemoglobin, Lactate, Vasopressor / inotrope doses and Sedation score (RASS). 5. Echocardiography parameters: recorded every 12 hours. LV ejection fraction. LVOT VTi. LVED dimension. Aortic valve opening. 6. Follow-up data:

* ECMO duration. * Need for oxygen therapy/mechanical ventilation. * ICU survival.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Patients supported with veno-arterial ECMO.

Presence of a pulmonary artery catheter.

Expected ECMO support ≥ 24 hours.

Disqualifiers

Pre-existing severe neurological injury (e.g. massive stroke, traumatic brain injury).

Intracranial pathology affecting NIRS reliability.

Facial or scalp conditions preventing NIRS probe placement.

ECMO duration < 48 hours.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Locations

This trial has no locations

Sponsors and collaborators

Assiut University

Lead sponsor

Cairo University/ECMO unit

Collaborator