Development and Validation of a Prognostic Model for Neurocritical Patients Using Multimodal Brain Monitoring

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorXiangya Hospital of Central South University

About this trial

This study aims to develop and validate a prognostic model for neurocritical patients using multimodal brain monitoring data. By combining data from various monitoring techniques such as EEG, TCD, and NIRS, this model will help predict 90-day outcomes (awake, comatose, or deceased) and support personalized treatment decisions. The study is observational and involves no experimental interventions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 18-80 years, no gender restrictions.

Diagnosed with acute brain injury (ABI), including one of the following: large cerebral infarction, supratentorial large-volume intracerebral hemorrhage, subarachnoid hemorrhage, or severe traumatic brain injury, with imaging evidence (CT or MRI) supporting the diagnosis.

On ICU admission, Glasgow Coma Scale (GCS) eye response = 1 (no eye opening) and motor score ≤ 5 (does not follow commands); or within 48 hours, neurological deterioration with no eye opening and motor score reduced to ≤ 5 (total GCS score ≤ 8).

Able to undergo continuous multimodal monitoring, with an expected ICU stay of ≥72 hours.

Disqualifiers

Confirmed brain death on admission or imaging showing irreversible brain herniation.

Severe trauma unrelated to brain injury (e.g., multiple fractures, spinal cord injuries, or visceral rupture) that may interfere with brain function monitoring or outcome assessment.

Pre-existing severe neurological disorders such as epilepsy, severe encephalopathy, or chronic intracranial conditions (e.g., brain tumors or hydrocephalus).

Inability to perform multimodal monitoring due to technical issues (e.g., equipment failure or sensor installation problems).

Trial population

Neurocritical patients aged 18-80 years with acute brain injury admitted to the ICU.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

90-day Outcome Prediction

The primary outcome is the prediction of patient status at 90 days post-ICU admission, categorized as awake, comatose, or deceased.

Time frame
90-day

Secondary outcomes

Other outcomes

Sponsors and contacts

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