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RecruitingNCT06504238NIMABIUpdated Sep 30, 2026

Non-Invasive Monitoring Methods in Patients With Acute Brain Injury

An observational study in Brain Injury, Acute, sponsored by Boston Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-30.

Sponsored by Boston Medical Center · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
720
Ages
18 Years and older
Sex
All
01

Study summary

Life-threatening mass effect (LTME) arises when brain swelling displaces or compresses crucial midline structures subsequent to acute brain injuries (ABIs) like traumatic brain injury (TBI), ischemic stroke (IS), and intraparenchymal hemorrhage (IPH), which can manifest rapidly within hours or more gradually over days. Despite advancements in surgical management, significant gaps in understanding persist regarding optimal monitoring and therapeutic approaches. The current standard for identifying LTME involves neurologic decline in conjunction with radiographic evidence or increased intracranial pressure (ICP) indicating space-occupying mass effect. However, in critically ill patients, reliance on subjective physical exam findings, such as decreased arousal, often leads to delayed recognition, occurring only after catastrophic shifts have already occurred.

The goal of this study is to determine the association of non-invasive biomarkers with neurologic deterioration, and to determine whether non-invasive biomarker inclusion improves detection of outcome and decline.

The investigators propose to use various non-invasive methods to monitor ICP as adjuncts in detecting deteriorating mass effect. These methods include quantitative pupillometry, radiographic data, laboratory data, and other bedside diagnostic tests available including electroencephalography (EEG), skull vibrations detected via brain4care device, optic nerve sheath diameter assessment (ONSD), and ultrasound-guided eyeball compression. Some of these methods will be measured *only* for the purposes of the research study (such as skull vibrations via brain4care). Other measurements, such as quantitative pupillometry, will represent additional measurements beyond those already being collected for clinical care. This research study is necessary to understand the association of these non-invasive biomarkers with neurological decline and outcomes while considering potential confounding factors.

02

Conditions studied

  • Brain Injury, Acute

Keywords

  • Life-threatening mass effect (LIME)
  • Traumatic brain injury (TBI)
  • Ischemic stroke (IS)
  • Intraparenchymal hemorrhage (IPH)
  • Neurologic deterioration
  • Intracranial Pressure (ICP)
  • Glasgow Coma Scores
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Eligible patients will be recruited on admission to the intensive care unit (ICU) at Boston Medica Center followed by the Neurointensive care team.

Inclusion criteria

  • Admitted under Neuro intensivist primary or consultative care.
  • At least one head computed tomography (CT) scan demonstrating intracranial pathology that may lead to life-threatening mass effect (i.e. traumatic brain injury, ischemic or hemorrhagic stroke, epidural or subdural hematoma, subarachnoid hemorrhage, diffuse hypoxic injury, metabolic cerebral edema, tumor)
  • Concern for Life Threatening Mass Effect
  • Glasgow Coma Score (GCS) \<9
  • Anticipated stay >24 hours

Exclusion criteria

Exclusion Criteria:

  • Comfort measure only
  • Any other criteria that the PI deems that makes the patient inadequate for the study
  • Sub-exclusion criteria for specific non-invasive measurements include:

    • Orbital injury (pupillometry, ONSD)
    • Traumatic injury or surgery that precludes use of B4C device
  • Presence of supratentorial craniectomy or craniotomy that has not healed and is mobile/bone defects/scalp injury [EEGelectroencephalogram (EEG), Brain4Care]
  • Presence of extensive scalp injury
04

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
720 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • NIMABI Group

    Eligible patients will be recruited on admission to the ICU followed by the Neurointensive care team. Demographic, invasive ICP monitoring data, clinical, laboratory, diagnostic, treatment (medical and surgical) and outcome data will be collected. Data will be collected from non-invasive devices using either clinical review from the chart, or if not available and/or used for additional measurements, from the device (smartguard for pupillometry, imaging, EEG data, Brain4care data).

05

What researchers measure

Primary outcomes

  1. Neurologic Deterioration

    Neurologic deterioration will be assessed as a dichotomous variable (yes/no) defined as a negative change in any of the following: level of consciousness, agaze, arm motor function, leg motor function, or language. The participants' medical chart will be reviewed for documentation of persistent change.

    Time frame: 5 years

  2. Glasgow Coma Scores

    The Glasgow Coma Scale (GCS) is a 15-point scale used to evaluate a person's state of consciousness. A score of 3 is the lowest possible and indicates a deep coma or death, while a score of 15 is the highest and indicates a fully awake person. A lower score generally means a deeper coma.

    Time frame: 5 years

Secondary outcomes

  1. Number of participant deaths during hospitalization

    This data will be abstracted from medical records..

    Time frame: 5 years

  2. Functional outcome at hospital discharge

    This will be assessed by Modified Rankin Scale (mRS), a 6 point disability scale with possible scores ranging from 0 to 5, higher scores indicating greater disability and where 0-2 is generally considered a good outcome with individuals assuming complete functional independence. A separate category of 6 is usually added for patients who expire. Data will be abstracted from medical records on review of patient notes and discharge summaries to obtain amRS for each participant.

    Time frame: 5 years

06

Study locations

1 of 1 sites recruiting
  • Boston Medical Center
    Boston, Massachusetts 02118, United States
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06504238
Lead sponsor
Boston Medical Center
Responsible party
Sponsor
First posted
Jul 16, 2024
Start date
Sep 26, 2024
Primary completion
Sep 2030 (estimated)
Completion
Sep 2030 (estimated)
Last update
Sep 30, 2026

Study contacts

Charlene Ong, MD MPHS
Contact
cjong@bu.ed
617 638 5351
Leigh Mallinger, BA
Contact
leigh.mallinger@bmc.org
617-638-7732
Charlene Ong, MD MPHS
principal investigator · Boston Medical Center, Neurology

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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