- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04464824
Study of the Preventable Passage of Patients Over 75 Years of Age to the Emergency Room of the CHRU of Nancy (PE75UN)
The adult emergency service of the Nancy CHRU welcomes an average of 135 visits per day. Approximately 18% are patients over 75 years old, among them 45% go home at the end of their care. The mobile geriatric liaison team intervenes with these patients at the request of the emergency doctors before they return home in order to identify their fragility and implement appropriate measures.
We wish to know the characteristics of these avoidable passages in order to propose preventive measures upstream of these passages. To do this, we need to know the characteristics of those patients with an avoidable passage.
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Nancy, France
- CHRU de Nancy
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- age>=75 years old
- admitted at emergency room between first april 2019 and 30 september 2019
- outpatients
Exclusion Criteria:
- inpatients
- discharged patients
- patients discharged against medical advice
- patients brought by police
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
patient over 75 years of age with an emergency room visit
Patients over 75 years of age, with a visit to the emergency department between April 1, 2019 and September 30, 2019, with a non-hospitalization at the end of their visit to the emergency department.
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no intervention
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
characteristics of preventable passages to the emergency room of the Nancy CHRU in the population over 75 years old
Time Frame: the day of the admission at emergency room
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the day of the admission at emergency room
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020PI066
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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