- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02827825
Patients Undergoing Strokes Admitted in Intensive Care Requiring Neurosurgical ICU Crossing: Patient Profile and Prognosis
April 26, 2023 updated by: Groupe Hospitalier Paris Saint Joseph
The aim of this study is to describe the population of patients admitted to the ICU in neurosurgery for stroke requiring secondary care in intensive care and their future.
Study Overview
Detailed Description
Methodology :
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
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Ile-de-France
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Paris, Ile-de-France, France, 75014
- Groupe hospitalier Paris saint Joseph
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients admitted in Intensive Care Requiring Neurosurgical for ischemic or hemorrhagic stroke.
then, admitted secondarily in ICU
Description
Inclusion Criteria:
- Admitted USINV for ischemic or hemorrhagic stroke
- Admitted secondarily in ICU
Exclusion Criteria:
- Admission in ICU in first
- 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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Death event
Time Frame: Day 1 after hospitalization
|
Day 1 after hospitalization
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: ZUBER Mathieru, MD, Groupe hospitalier Paris saint Joseph
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2015
Primary Completion (Actual)
January 1, 2016
Study Completion (Actual)
January 1, 2016
Study Registration Dates
First Submitted
June 30, 2016
First Submitted That Met QC Criteria
July 6, 2016
First Posted (Estimate)
July 11, 2016
Study Record Updates
Last Update Posted (Actual)
April 27, 2023
Last Update Submitted That Met QC Criteria
April 26, 2023
Last Verified
June 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AVC REANIMATION
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.