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

Status

Completed

Conditions

Intervention / Treatment

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

    • Ile-de-France
      • Paris, Ile-de-France, France, 75014
        • Groupe hospitalier Paris saint Joseph

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

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.

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