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Multimodal Monitoring Study in Neuro Critical Care

Multimodal Monitoring Study in Neuro Critical Care

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06900101
Acronym
MultiCU
Enrollment
500
Registered
2025-03-28
Start date
2020-01-01
Completion date
2030-12-01
Last updated
2025-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Trauma Brain Injury, Intacranial Hypertension, Subarachnoidal Hemorrhage

Brief summary

During the first week after an acute cerebral injury, neurologic clinical exam is often irrelevant, limited by sedation use or spontaneous consciousness disorders. Hence, neurological monitoring of brain oxygen consumption, metabolic disorders, electrical activity is used to follow and prevent delayed cerebral injuries. Among those instruments, numerous are often described: intra cranial pressure monitoring, brain tissue oxygen pressure monitoring, scalp electroencephalography, continuous electroencephalography and Near infrared Red Spectroscopy (NIRS). Even if the value of some of those technologies are well known, many remain part of a research domain. Here we will not only try to study the correlation between different cerebral autoregulation's index described in the scientific literature but also will we try to identify and describe EEG and cardiorespiratory changes during the first week following brain injury. The objective of this study is to investigate the pathophysiology of acute brain injury and explore potent biomarkers of multimodal monitoring during the first week following acute brain injury.

Interventions

OTHERStudy the evolution and correlation between cerebral autoregulation index

Objective n°1: Study the correlation between autoregulation index: The investigators will look for a correlation between several auroregulation index such as the PRx, ORx and Cox. Objective n°2: Evaluation and detection of EEG prognostic patterns: The investigators will look for quantitaive EEG changes during the early phase of acute brain injuries.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* \- Patients hospitalized in neurologic critical care in Wertheimer Hospital, Bron * Monitored with the CNS MOBERG® monitoring system

Exclusion criteria

* \- Refusal to participate * Patients under legal protection

Design outcomes

Primary

MeasureTime frame
Correlation between ORx and PRxMultimodal neuro monitoring is used from 1 to 15 days after the acute brain injury.

Countries

France

Contacts

Primary ContactDr Baptiste Balança
baptiste.balanca@chu-lyon.fr04 72 35 75 76

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026