Patients Undergoing Strokes Admitted in Intensive Care Requiring Neurosurgical ICU Crossing: Patient Profile and Prognosis

Cerebral Stroke Clinical Trial

Official title:

Patients Undergoing Strokes Admitted in Intensive Care Requiring Neurosurgical ICU Crossing: Patient Profile and Prognosis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02827825
• Other study ID #: AVC REANIMATION
• Status: Completed
• 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
• 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

Related Conditions & MeSH terms

• Cerebral Stroke
• Stroke

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