Actively Recruiting

Age: 18Years - 100Years
All Genders
NCT05303363

Monitoring of Cerebral Blood Flow in Patients on Extracorporeal Membrane Oxygenation

Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-08-15

15

Participants Needed

1

Research Sites

191 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Venovenous extracorporeal membrane oxygenation (VV-ECMO) is a supportive therapy, indicated in case of severe, possibly reversible pulmonary failure, refractory to conventional therapies. Despite advances, morbidity and mortality remain high. Severe neurological complications can occur during ECMO, but their exact etiology is not well understood. It is hypothesized that fast correction of severe hypercapnia, a common indication for venovenous ECMO, may be detrimental for the brain. The supposed mechanism is that fast correction of hypercapnia may result in massive cerebral vasoconstriction and impaired cerebral blood flow (CBF). In this prospective, observational study the aim is to quantify change in CBF during routine initial correction of severe hypercapnia during VV-ECMO. Furthermore, the investigators will record any other hemodynamic changes during VV-ECMO. The hypothesis is that a larger decline in PaCO2 will result in a larger decline of CBF.

CONDITIONS

Official Title

Monitoring of Cerebral Blood Flow in Patients on Extracorporeal Membrane Oxygenation

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • High suspicion of an indication for VV-ECMO
  • Arterial line present to enable blood sampling
  • Older than 18 years
Not Eligible

You will not qualify if you...

  • Cerebral blood flow cannot be measured using transcranial Doppler
  • Receiving VA-ECMO or extracorporeal cardiopulmonary resuscitation (ECPR)
  • Neuromonitoring measurements not possible due to technical difficulties (e.g., post-craniotomy, unsuitable transcranial window)
  • Neuromonitoring measurements not possible due to circumstantial difficulties (e.g., ECPR)
  • Contraindications for ECMO
  • ECMO initiated in another center

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Amsterdam UMC

Amsterdam-Zuidoost, Netherlands, 1105

Actively Recruiting

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Research Team

A

Alexander Vlaar, MD PhD MBA

CONTACT

R

Rogier Immink, MD PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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