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NCT01903746 Clinical Trial

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

Severe Sepsis Clinical Trial

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT01903746
Other study ID # Quenot PHRC IR 2008
Secondary ID
Status Terminated
Phase N/A
First received July 17, 2013
Last updated July 17, 2013
Start date October 2010
Est. completion date January 2011

Study information
Verified date July 2013
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority France: Comité consultatif sur le traitement de l'information en matière de recherche dans le domaine de la santéFrance: Committee for the Protection of Personnes
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Terminated
Enrollment 1495
Est. completion date January 2011
Est. primary completion date January 2011
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

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

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Outcome
Type Measure Description Time frame Safety issue
Primary Sequential Organ Failure Assessment baseline No
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