Patients Undergoing Strokes Admitted in Intensive Care Requiring Neurosurgical ICU Crossing: Patient Profile and Prognosis
NCT ID: NCT02827825
Last Updated: 2023-04-27
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
50 participants
OBSERVATIONAL
2015-09-30
2016-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Observational Study of Patients With Subarachnoid Hemorrhage
NCT02890004
Strokecopilot: A Precision Medicine Tool in the Stroke Emergency
NCT05534295
Follow-up of Malnutrition Screening in USINV
NCT03728400
Stroke Prognosis in Intensive CarE
NCT03335995
Functional Prognosis in Patients With Ischemic Stroke According to the Therapeutic Strategy Used
NCT02856074
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
DESIGN:
Retrospective observational study single center, non-interventional Term study over 2 years, retrospectively
Acquisition of data:
* Study of computer file: report available on DxCare hospital and Cora
* Collection of data as excel spreadsheet
* Statistical analysis: local management
* Anonymity of data:
* For each subject will be awarded an identifier (original name and surname - year of birth) and the data will be entered on a computer file which will be sent to the statistician in charge of analyzing the GHPSJ site. There will be no exchange of personal data for this study is single center on the site GHPSJ.
Development of the study:
* Procedure:
* Series includable patients from the PMSI data
* Select folders according the inclusion criteria
* Collecting information from files on Excel spreadsheet by the internal charge of data collection (Sylvain CHAWKI)
* Statistical Analysis
* Writing Article
* Expected duration of patient recruitment: Retrospective of 2 and a half years from January 1, 2013 to April 31, 2015
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
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
No intervention
No intervention. It's a study on retrospective Data
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Admitted secondarily in ICU
Exclusion Criteria
* Administrative Admission in Intensive Care Requiring Neurosurgical within the thrombolysis alert regulated by the neurovascular guard but going directly to ICU imaging waning
* Subarachnoid hemorrhage
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Fondation Hôpital Saint-Joseph
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
ZUBER Mathieru, MD
Role: PRINCIPAL_INVESTIGATOR
Fondation Hôpital Saint-Joseph
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Groupe Hospitalier Paris Saint Joseph
Paris, Île-de-France Region, France
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.
AVC REANIMATION
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.