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NCT06900101Recruiting

Multimodal Monitoring Study in Neuro Critical Care

Source: ClinicalTrials.gov · Last updated 28 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
21 Mar 2025
Start date
1 Jan 2020
Primary completion date
1 Dec 2030
Lead sponsor
Hospices Civils de Lyon
NCT number
NCT06900101

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 1 Jan 2020 to the primary completion date, 1 Dec 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \- Refusal to participate
  • Patients under legal protection

Who the study is looking for

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

Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Pierre Wertheimer
Coordinator of this site? Confirm its status
FranceFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.