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

NCT ID: NCT01903746

Last Updated: 2013-07-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

1495 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-10-31

Study Completion Date

2011-01-31

Brief Summary

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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.

Detailed Description

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Conditions

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Severe Sepsis Persistent Hypotension

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients in septic shock

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* None
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire Dijon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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jean pierre Quenot

Role: PRINCIPAL_INVESTIGATOR

department Medical Intensive Care

Other Identifiers

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Quenot PHRC IR 2008

Identifier Type: -

Identifier Source: org_study_id

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