- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02307136
Evaluation of the Impact of Within-hospital Trajectories of Patients Admitted in Intensive Care Units (ICU) From Emergency Departments (SUREA)
This multicenter cohort aims to assess the impact of within-hospital trajectories of patients admitted in intensive care units from emergency departments on vital prognosis of patients, duration of hospital stay and hospital costs.
As secondary objectives, the study will:
- assess the impact of clinical and demographic characteristics on hospital trajectories of patients.
- assess the impact of emergency units workload, beds availability in medical units and in intensive care units, and global hospital organisation on patients care trajectories.
Study Overview
Status
Conditions
Detailed Description
The study will be performed in emergency departments and ICUs of university hospitals. 15 emergency departments and 36 ICUs of APHP (the public hospital system of the city of Paris) will be involved.
The study will assemble the data from 50,000 to 80,000 patients in total.
Eligible patients are admitted in ICUs between 01/01/2007 and 12/31/2011.
Extraction of the patients' data will be performed with processing software utilised in APHP, i.e. Healthcare Information System Program (PMSI, Urqual, Gilda...etc.).
Collected patients' data span the period from admission in emergency department or medical department unitl hospital discharge.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Île-de-France
-
Paris, Île-de-France, France, 75018
- Emergency Department, Bichat-Claude Bernard Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult patient directly admitted in ICU from emergency departments of APHP (the public hospital system of the city of Paris).
- Adult patient indirectly transferred to ICU from an hospitalization unit, initially admitted from an emergency department of APHP.
Exclusion Criteria:
- Patient transferred from APHP toward an external hospital, outside APHP, before being admitted in an ICU.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mortality
Time Frame: throughout the study: 5 years
|
Mortality in ICU and in other hospital units
|
throughout the study: 5 years
|
|
Rate of direct transfer
Time Frame: throughout the study: 5 years
|
Rate of direct transfer from Emergency Unit to ICU
|
throughout the study: 5 years
|
|
Rate of indirect transfer
Time Frame: throughout the study: 5 years
|
Rate of indirect transfer from a hospitalization Unit to ICU
|
throughout the study: 5 years
|
|
Duration of stay in emergency department, in ICU and in hospital
Time Frame: throughout the study: 5 years
|
Duration of stay in emergency department, in ICU and in hospital
|
throughout the study: 5 years
|
|
Mode of discharge from ICU
Time Frame: throughout the study: 5 years
|
Mode of discharge from ICU and direction of patient (home, other structures etc.)
|
throughout the study: 5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Severity scores
Time Frame: throughout the study: 5 years
|
Severity scores in ICU
|
throughout the study: 5 years
|
|
Use and duration of mechanical ventilation
Time Frame: throughout the study: 5 years
|
Use and duration of mechanical ventilation for patient during ICU stay
|
throughout the study: 5 years
|
|
Score of burden of care in ICU
Time Frame: throughout the study: 5 years
|
Score of burden of care in ICU
|
throughout the study: 5 years
|
|
Percentage of patients with ICU stay
Time Frame: throughout the study: 5 years
|
Percentage of patients with ICU stay
|
throughout the study: 5 years
|
|
Percentage of patients with continuing care
Time Frame: throughout the study: 5 years
|
Percentage of patients with continuing care after discharge from the ICU
|
throughout the study: 5 years
|
|
Frequency of dialysis
Time Frame: throughout the study: 5 years
|
Frequency of dialysis
|
throughout the study: 5 years
|
Collaborators and Investigators
Investigators
- Principal Investigator: Enrique CASALINO, MD, PhD, APHP
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NI11013-AOR11114
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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