Long-term Effects of Time to Treatment in Subarachnoid Haemorrhage
NCT ID: NCT04377347
Last Updated: 2021-02-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
537 participants
OBSERVATIONAL
2020-05-01
2021-02-24
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This is a retrospective cohort study with four-year followup. The primary aim is to determine if the time to neurosurgical admission is associated to labour marked affiliation and mortality after four years.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Time to Specialized Admission in Case of Severe Brain Haemorrhage.
NCT03786068
Presentation of Subarachnoid Haemorrhage
NCT03980613
Prehospital Deaths From Spontaneous Subarachnoid Haemorrhages
NCT04052646
MicroRNA Diagnostics in Subarachnoid Hemorrhage
NCT01791257
Cerebral Autoregulation in Patients With Aneurysmal SubArachnoid Haemorrhage
NCT03987139
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
OTHER
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Confirmed spontaneous subarachnoid haemorrhage
Patients, minimum 18 years of age, identified with the diagnosis in the Danish National Patient Register. The diagnosis is verified by medical record review.
All patients were initially admitted to a hospital in the Capital Region of Denmark.
In a national labour marked register and the civil registration register the patients are then followed for four years.
Time
Exposure is the time from patients call the Emergency Medical Coordination Center to they are admitted to a neurosurgiocal department.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Time
Exposure is the time from patients call the Emergency Medical Coordination Center to they are admitted to a neurosurgiocal department.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Initially admitted to a hospital in the Capital Region of Denmark between 1 January 2008 and 31 December 2014.
Exclusion Criteria
* Inhospital symptom onset.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Rigshospitalet, Denmark
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Asger Sonne, MD
Principal investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Rigshospitalet
Copenhagen, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Outcome
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.