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

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01903746
Enrollment
1495
Registered
2013-07-19
Start date
2010-10-31
Completion date
2011-01-31
Last updated
2013-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Persistent Hypotension, Severe Sepsis

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.

Interventions

None listed

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
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

* None

Design outcomes

Primary

MeasureTime frame
Sequential Organ Failure Assessmentbaseline

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026