Status:
UNKNOWN
Blood Lactate Level for Pre-hospital Orientation of Septic Shock
Lead Sponsor:
Hôpital Necker-Enfants Malades
Collaborating Sponsors:
Fire Brigade Of Paris Emergency Medicine Dept
University Hospital, Grenoble
Conditions:
Sepsis
Lactate Blood Increase
Eligibility:
All Genders
18+ years
Brief Summary
In the pre-hospital setting, the severity assessment of septic shock is essential to decide the optimal initial in-hospital level of care. As clinical signs can be faulted, there is a need for an addi...
Detailed Description
This trial is a prospective, observational, non-randomized controlled study. A total of 1000 patients requiring mobile intensive care unit intervention for a septic shock in the pre-hospital setting w...
Eligibility Criteria
Inclusion
- Age \> 18 years either sex
- Severe sepsis according to the French anesthesiology and intensive care society (SFAR) and intensive care society (SRLF) conference 2005 defined by the existence of an infectious disease and at least one the following:
- Low blood pressure prior to volume expansion
- Glasgow coma scale \< 13
- Skin mottling score \> 2
- Septic shock according to the French anesthesiology and intensive care society (SFAR) and intensive care society (SRLF) conference 2005 definition
Exclusion
- Age \< 18 years
- Pregnancy
- Serious comorbid conditions with a not to be reanimated status known since pre-hospital setting
- Patients with guardianship or curator
Key Trial Info
Start Date :
March 1 2018
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
March 1 2022
Estimated Enrollment :
1000 Patients enrolled
Trial Details
Trial ID
NCT03831685
Start Date
March 1 2018
End Date
March 1 2022
Last Update
February 11 2019
Active Locations (1)
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1
APHP Necker Enfants Malades
Paris, France, 75015