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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02827825
Other study ID # AVC REANIMATION
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2015
Est. completion date January 2016

Study information

Verified date June 2016
Source Groupe Hospitalier Paris Saint Joseph
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date January 2016
Est. primary completion date January 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention
No intervention. It's a study on retrospective Data

Locations

Country Name City State
France Groupe Hospitalier Paris Saint Joseph Paris Ile-de-France

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Death event Day 1 after hospitalization
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