NCT07052656

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2010

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
15 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

May 28, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 4, 2025

Completed
Last Updated

July 10, 2025

Status Verified

July 1, 2025

Enrollment Period

15 years

First QC Date

May 28, 2025

Last Update Submit

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

Other: Observational study, participants are not assigned an intervention as part of the study.Other: Transport modality

Interventions

Observational study, participants are not assigned an intervention as part of the study.

Neuro-intensive care patients

Transfer modality to tertiary centers

Neuro-intensive care patients

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Karolinska University Hospital

Stockholm, Sweden

Location

MeSH Terms

Conditions

Subarachnoid HemorrhageIschemic StrokeCerebral HemorrhageStrokeMeningitisEpilepsyBrain Injuries, TraumaticBrain Injuries

Interventions

Observation

Condition Hierarchy (Ancestors)

Intracranial HemorrhagesCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesHemorrhagePathologic ProcessesPathological Conditions, Signs and SymptomsNeuroinflammatory DiseasesCraniocerebral TraumaTrauma, Nervous SystemWounds and Injuries

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

Study Officials

  • Linn Hallqvist, MD, PhD

    Dep of Perioperative Medicine and Intensive care, Karolinska University Hospital

    PRINCIPAL INVESTIGATOR

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

Locations