- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03280992
Community Acquired Sepsis Cohort (CASC)
December 1, 2021 updated by: Rennes University Hospital
The aim of this project is to constitute a prospective cohort of all the patients presenting to the adult emergencies of the University Hospital Centre (CHU) of Rennes for a septic syndrome of community origin.
Study Overview
Status
Terminated
Conditions
Detailed Description
Severe septic syndrome (SSG) and septic shock (CS) are two frequent and serious complications of infectious diseases.
In this context, the optimization of the management of septic patients from their reception in the emergency services must be a priority.
However there are no predictors of progression or severity in patients admitted to emergencies despite the recommendations emphasizing the need for screening and early therapeutic management.
Many scores have been proposed for intensive care unit but they remain difficult to extrapolate to other services because they are very comprehensive and require information that is difficult to obtain for emergency physicians.
Study Type
Observational
Enrollment (Actual)
796
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Rennes, France, 35033
- CHU de Rennes
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patient with a community infectious diseases
Description
Inclusion Criteria:
- Patient older than 18 years old
- Patient hospitalized during the study period for community infectious diseases at the CHU of Rennes
Exclusion Criteria:
- Written objection from the patient to the computer processing of his data
- Pregnant women
- Persons subject to major legal protection (safeguarding justice, guardianship, trusteeship), persons deprived of liberty
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of morbidity in patients with septic syndrome of community origin
Time Frame: Day 90
|
Study of prognostic factors
|
Day 90
|
|
Internal validity, severity score
Time Frame: Day 90
|
Day 90
|
|
|
Internal validity, triage score by orientation nurses
Time Frame: Day 90
|
Day 90
|
|
|
Study of the prognostic factors of patients with septic syndrome of community origin in terms of mortality
Time Frame: Day 90
|
Day 90
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
March 2, 2016
Primary Completion (ACTUAL)
August 27, 2018
Study Completion (ACTUAL)
August 27, 2018
Study Registration Dates
First Submitted
August 18, 2017
First Submitted That Met QC Criteria
September 12, 2017
First Posted (ACTUAL)
September 13, 2017
Study Record Updates
Last Update Posted (ACTUAL)
December 2, 2021
Last Update Submitted That Met QC Criteria
December 1, 2021
Last Verified
December 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 35RC16_3024_CASC
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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