Understanding Outcomes for Life-Threatening Neurologic Illness

This observational study aims to better understand life-threatening brain illnesses like intracerebral hemorrhage (bleeding in the brain) and status epilepticus (prolonged seizures). Researchers are looking at how these conditions affect the brain and how standard medical care might impact recovery. They are collecting information from patients admitted to the NeuroCritical Care Unit to see how different factors, including complications like fever or infections, influence long-term outcomes. Success in this study will be measured by how well participants recover their daily living skills, thinking abilities, and overall independence three months after their illness. This study is currently unclear on its recruitment status.

Study design
This is an observational study, meaning researchers are collecting information without providing any specific intervention. It plans to include up to 5000 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants' recovery is assessed at three months after their illness.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04189471

Improving Outcomes for Patients With Life-Threatening Neurologic Illness

Recruiting
Not specifiedAges 18+Observational
University of Maryland, Baltimore
~5,000 participants
Updated 2026-07-02 on ClinicalTrials.gov

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of participants who score great than 60 on the Barthel Index
Measured over 3 month
+4 more outcomes measured
Intracerebral Hemorrhage
Subarachnoid Hemorrhage
Intraventricular Hemorrhage
Nontraumatic Haemorrhage
Status Epilepticus
1 sites across 1 states
Maryland1
  • Gunjan Y Parikh, MD · PRINCIPAL_INVESTIGATOR · University of Maryland, Baltimore

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

clinical diagnosis of potentially life-threatening neurological illness
admitted to Neuro ICU within 14 days of initial injury

Exclusion

known pre-existing neurological deficits related to a developmental disorder
prior severe stroke
prior severe dementia
prior severe head injury
prisoners
  • Number of participants who score great than 60 on the Barthel Index3 month

    The Barthel scale is an ordinal scale used to measure performance in activities of daily living. Scores range from 0 to 100. A higher score signifies better outcomes, more independent functionality.

  • Number of participants who score great than 26 on the Montreal Cognitive Assessment (MoCA)3 month

    The Montreal Cognitive Assessment was developed as a quick screening tool for neurological function. It assesses the domains of attention and concentration, executive function, memory, language, visuoconstructional skills, conceptual thinking, calculation, and orientation. The MoCA has been tested extensively for use in a variety of disorders affecting cognition such as HIV, Huntington's chorea, Multiple Sclerosis, Parkinson's disease, stroke, vascular dementia, and substance abuse in addition to the wellness of older adults. The MoCA has been tested in ages ranging from as young as 49 in two reports to old-old (85+) with a variety of education levels. The total possible score is 30 points with a score of 26 or more considered normal.

  • Number of participants who score 1 or less on the Modified Rankin Scale3 month

    The Modified Rankin Scale (mRS) measures degree of disability/dependence after a stroke. Scores range from 0 to 6. A lower score signifies better outcomes, more independent functionality.

  • Number of participants who have experienced adverse events3 month

    Medical history from hospital discharge to three months will help researchers learn of any adverse events or other medical complications.

  • Number of participants who score great than 75 on the EuroQOL3 month

    EQ-5D is a standardised measure of health status developed by the EuroQol Group in order to provide a simple, generic measure of health for clinical and economic appraisal. The EQ-5D questionnaire also includes a Visual Analog Scale (VAS), by which respondents can report their perceived health status with a grade ranging from 0 (the worst possible health status) to 100 (the best possible health status).