- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06288295
Retrospective Study on Data Aiming to Establish a Prediction Score for Return Home at the Time of Admission to a Multidisciplinary Medical Department (SCORDOM (SCORDOM)
Retrospective Study on Data Aiming to Establish a Prediction Score for Return Home at the Time of Admission to a Multidisciplinary Medical Department
The goal of this observational study is to define clinical, biological and socio-cultural criteria, from the very first days of hospitalization on the multidisciplinary medicine department, to guide the patient's discharge from hospital (return to home when discharged from hospital).
The data collected will be those contained in the medical records of patients over 60 years of age who were admitted to the multidisciplinary medical department between October 2021 and February 2022 and between October 2022 and February 2023.
This study also aims at developing and validating a predictive score of orientation at the end of hospitalisation.
Participants are patients previously hospitalized. They will be informed about the study by post and will be able to object to the use of his or her data.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Nancy, France, 54000
- Hôpital Privé Nancy Lorraine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
For the development of the score:
- All patients over 60 years of age admitted to the multidisciplinary medical department in the investigating center between October 2021 and February 2022.
- Patients for whom data of interest to this study are available in medical records.
For score validation :
- All patients aged over 60 admitted to the multidisciplinary medicine department of the investigating center between October 2022 and February 2023.
- Patients for whom data of interest to this study are available in medical records.
Exclusion Criteria:
- Patients transferred from an intensive care or continuing care unit
- Patients in palliative care
- Patients residing in an EHPAD (establishment for the elderly) or nursing home prior to hospitalization
- Patients without a minimum blood test on admission (blood test less than 48 hours old)
- Patients whose reason for hospitalization is due to COVID
- Patients who have objected to the use of their personal data
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Score development cohort
Patients over 60 years of age admitted to a general medicine department in the investigating center between October 2021 and February 2022
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Score validation cohort
Patients over 60 years of age admitted to a general medicine department in the investigating center between October 2022 and February 2023
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of patients with a return to home after hospitalization and with similar clinical parameters, similar age category, similar pathology and similar biological parameters
Time Frame: Hospital stay, up to 3 weeks
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Data collected among hospital data from october 2021 to february 2022.
Clinical parameters measured: age, confusional syndrome, fever, eschar, blood pressure, etc; biological paremeters: (blood test performed in the last 2 days before discharge: albuminemia, natremia, protein C, Creatinemy, hemoglobinemy)
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Hospital stay, up to 3 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of patients with a return to home after hospitalization and with similar clinical parameters, similar age category, similar pathology and similar biological parameters
Time Frame: Hospital stay, up to 3 weeks
|
Data collected among hospital data from october 2022 to february 2023.
Clinical parameters measured: age, confusional syndrome, fever, eschar, blood pressure, etc; biological paremeters: (blood test performed in the last 2 days before discharge: albuminemia, natremia, protein C, Creatinemy, hemoglobinemy)
|
Hospital stay, up to 3 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Anais Bauer, PhD, Hôpital Privé Nancy Lorraine
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 (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Etude SCORDOM
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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