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Hospital Orientation Since SAMU Regulation Centre Call

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ClinicalTrials.gov Identifier: NCT03237403
Recruitment Status : Recruiting
First Posted : August 2, 2017
Last Update Posted : August 3, 2017
Sponsor:
Information provided by (Responsible Party):
Romain Jouffroy, Hôpital Necker-Enfants Malades

Brief Summary:
Specify the association between clinical criteria transmitted by non-medical emergency services to the regulation of the SAMU centre call in patients with suspected sepsis and their hospital orientation: emergency department or intensive care unit

Condition or disease Intervention/treatment
Sepsis Other: observational study

Detailed Description:
Anonymous, descriptive, longitudinal, resting study searching an association between clinical criteria transmitted by non-medical emergency services to the regulation of the SAMU centre call for patients with suspected sepsis and their subsequent hospital orientation

Study Type : Observational
Estimated Enrollment : 1000 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Study of Association Between Clinical Criteria Collected at the SAMU Regulation Centre Call and the Hospital Orientation of Patients With Suspected Sepsis State
Actual Study Start Date : January 1, 2017
Estimated Primary Completion Date : January 1, 2019
Estimated Study Completion Date : January 1, 2019

Resource links provided by the National Library of Medicine



Intervention Details:
  • Other: observational study
    observational study between clinical criteria collected at SAMU regulation centre call and hospital orientation


Primary Outcome Measures :
  1. Hospital Admission Service [ Time Frame: 1 day ]
    Emergency department or intensive care unit



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
All subjects calling the SAMU regulation centre call with a clinical suspected sepsis history
Criteria

Inclusion Criteria:

  • adults (age>18years)
  • patients with suspected sepsis state at the regulation SAMU centre call

Exclusion Criteria: minor (age<18years)


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03237403


Contacts
Contact: Romain Jouffroy, MD +3314495989 romain.jouffroy@aphp.fr
Contact: Benoit Vivien, MD, PhD +33144492424 benoit.vivien@aphp.fr

Locations
France
APHP Necker Enfants Malades Recruiting
Paris, France, 75015
Contact: Romain Jouffroy, MD    +3314495989    romain.jouffroy@aphp.fr   
Contact: Benoit Vivien, MD, PhD    +33144492424    benoit.vivien@aphp.fr   
Sponsors and Collaborators
Hôpital Necker-Enfants Malades
Investigators
Principal Investigator: Romain Jouffroy, MD APHP Necker Enfants Malades SAMU 75

Responsible Party: Romain Jouffroy, Principal Investigator, Hôpital Necker-Enfants Malades
ClinicalTrials.gov Identifier: NCT03237403     History of Changes
Other Study ID Numbers: 2017-A02335-48
First Posted: August 2, 2017    Key Record Dates
Last Update Posted: August 3, 2017
Last Verified: August 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: No IPD sharing plan is planned

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Romain Jouffroy, Hôpital Necker-Enfants Malades:
Sepsis
Adults
Pre hospital settings
Triage
Hospital orientation
Outcome

Additional relevant MeSH terms:
Sepsis
Infection
Systemic Inflammatory Response Syndrome
Inflammation
Pathologic Processes