Risk Factors and Outcomes in Patients Treated in Neurocritical Care
EpiNIC
2 other identifiers
observational
70,000
1 country
1
Brief Summary
The overall purpose of this epidemiologic research project is to provide a comprehensive exploration and analysis of critical elements within the neuro-intensive care process in Sweden. All aspects of intensive care management in critically ill patients with acute brain injury will be addressed. The analyses include description of patient characteristics, intensive care data, management and treatments, various aspects of short and long-term follow-up, mortality, regional- and sex-related differences. The long-term goal is to develop neuro-intensive care and management, to minimize in-hospital insults and secondary injuries, to improve diagnostics and follow-up, in order to reduce prolonged neurologic deficits and mortality in these patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2010
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedFirst Submitted
Initial submission to the registry
May 28, 2025
CompletedFirst Posted
Study publicly available on registry
July 4, 2025
CompletedJuly 10, 2025
July 1, 2025
15 years
May 28, 2025
July 4, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Mortality
Mortality
Up to two years
Secondary Outcomes (1)
Morbidity
Up to two years
Other Outcomes (2)
DAOH90
90 days
Complications
90 days
Study Arms (1)
Neuro-intensive care patients
Interventions
Observational study, participants are not assigned an intervention as part of the study.
Eligibility Criteria
All patients 18 years or older treated in an ICU in Sweden with a clinical diagnosis of subarachnoid hemorrhage, intracranial hemorrhage, ischemic brain injury, traumatic brain injury, epilepsy, meningitis, encefalitis or other brain injury diagnosis from 2010 to 2024.
You may qualify if:
- ICU admission 2010 to 2024
- Clinical diagnosis of subarachnoid hemorrhage, intracranial hemorrhage or ischemic brain injury, traumatic brain injury, epilepsy, meningitis, encefalititis or other brain injury diagnosis.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Karolinska Institutetlead
- Karolinska University Hospitalcollaborator
Study Sites (1)
Karolinska University Hospital
Stockholm, Sweden
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Linn Hallqvist, MD, PhD
Dep of Perioperative Medicine and Intensive care, Karolinska University Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 2 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD, PhD, Consultant, Principal Investigator
Study Record Dates
First Submitted
May 28, 2025
First Posted
July 4, 2025
Study Start
January 1, 2010
Primary Completion
December 31, 2024
Study Completion
December 31, 2024
Last Updated
July 10, 2025
Record last verified: 2025-07