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Clinical Trials/NCT01903746
NCT01903746TerminatedNot Applicable

Epidemiology of Septic Shock in Medical or Polyvalent ICU in the North-East Region of France

Centre Hospitalier Universitaire Dijon0 sites1,495 target enrollmentStarted: October 2010Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
1,495
Primary Endpoint
Sequential Organ Failure Assessment
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The epidemiology of this study aims and outcome of patients with septic shock in the intensive care unit (or versatile) of the North-East region in france as well as the modalities of care.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients in septic shock defined by hypotension that is not reversed by volume resuscitation and requires the use of vasopressors.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Sequential Organ Failure Assessment

Time Frame: baseline

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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