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Clinical Trials/NCT02714387
NCT02714387
Recruiting
Not Applicable

Prospective Cohort of Patients Hospitalized in West French Intensive Care Units.

Nantes University Hospital6 sites in 1 country5,000 target enrollmentFebruary 2013
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ConditionsNon Traumatic Acute Brain Injury

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non Traumatic Acute Brain Injury
Sponsor
Nantes University Hospital
Enrollment
5000
Locations
6
Primary Endpoint
in ICU stay complications
Status
Recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this observational epidemiological study is to investigate the management and the complications associated with Non Traumatic Neuro-Vascular Diseases. Data will be analysed to answer pre-defined scientific projects and to improve management of these conditions.

Detailed Description

Anonymous data will be collected by study coordinators in a secured e-database. Cross audit will be performed to check data.

Registry
clinicaltrials.gov
Start Date
February 2013
End Date
January 2050
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Non Traumatic Neuro-Vascular Diseases

Exclusion Criteria

  • •Consent withdrawal

Outcomes

Primary Outcomes

in ICU stay complications

Time Frame: Within the first 28 days after ICU admission date

Hospital acquired infections (epidemiology, risk factors, antibiotic susceptibility of pathogens), Organ failures (incidence, risks factors), Bleeding, Hemorrhage Intra-Cranial Hypertension, Brain Ischemia, Mechanical ventilation weaning, Extubation failure

Secondary Outcomes

  • Duration in mechanical ventilation(in ICU (up to 90 days))
  • ICU length of stay(in ICU (up to 90 days))

Study Sites (6)

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