Enhanced-contrast Brain Ultrasound in Cardiorespiratory Arrest
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- STATUS
- Recruiting
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- participants needed
- 100
-
- sponsor
- Universitair Ziekenhuis Brussel
Summary
Brain microcirculation alterations may be involved in
Description
Brain ultrasound, extracranial echo-color duplex and ocular ultrasound (IE 33, Philips
Medical System, the Netherlands) are performed in the first 24 hours, at 48 hours, and at
72-96 hours after successful
Ultrasound examinations are performed in four steps to 1) evaluate the global cerebral blood
volume, 2) to estimate the presence or absence of cerebral autoregulation, and 3) to
qualitatively evaluate the cerebral perfusion and microcirculation by enhanced microbubbles
contrast
Before performing brain ultrasound,
First, the global cerebral
Brain ultrasound is performed via temporal windows to measure the mean flow velocities (cm/sec) of the middle cerebral arteries.
Second, the presence or absence of cerebral autoregulation is tested with the Transient hyperemic response by an ipsilateral common carotid compression one side and another during 5 seconds. Absence of cerebral autoregulation is considered if the flow velocity of the middle cerebral artery do not increase more than 10% after the compression.
Third, the brain regional microcirculation is evaluated by the microbubbles contrast
All real-time images are stored digitally on the hard disk as DICOM (Digital Image
Communications in Medicine) images. Offline imaging analysis using a specific quantification
software named QLAB10 (Philips Medical System, the Netherlands) to convert
To qualitatively evaluate the intracranial pressure, ocular ultrasound is performed to
measure the change of the
Details
Condition |
Cardiac |
---|---|
Age | 18years - 85years |
Treatment |
|
Clinical Study Identifier | NCT04294316 |
Sponsor | Universitair Ziekenhuis Brussel |
Last Modified on | 19 February 2024 |
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Universitair ziekenhuis Brussel
Belgium
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Universitair ziekenhuis Brussel
Belgium
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Duc Nam Nguyen, MD, PhD
Primary Contact
Universitair ziekenhuis Brussel
Belgium
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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