- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05455892
Mortality, Gravity Predictive Factors and Clinical Evolution of Older COVID-19 Patients in Short Geriatric Services. (GERICOVID)
Analysis of Mortality, Gravity Predictive Factors and Evolution of Clinical Characteristics of Older Patients Hospitalized for COVID-19 in Short Geriatric Services.
Since the beginning of the year 2020, clinical characteristics of a new disease as the global COVID-19 epidemic has spread in France. People over 70 years of age are the more concerned by this virus in proportion and in gravity with some atypical first symptoms compared to younger patients. Evolution of the disease is variable from forms with few symptoms to severe forms sometimes quickly lethal.
GERICOVID LYON is a descriptive analysis of all patients over 70 years of age hospitalised for COVID-19 in short geriatric unities of University Hospital of Lyon This study will allow more comprehension about COVID-19 in older people. The role of predictive factors, pre-existing comorbidities and the nature and frequency of complications in a short period will be investigate. Treatments practices will be analysed too.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Rhone
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Caluire-et-Cuire, Rhone, France, 69300
- Service de gériatrie aigue de l'hôpital de la Croix Rousse. Hospices Civils de Lyon
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Lyon, Rhone, France, 69003
- Service de gériatrie aigue de l'hôpital Edouard Herriot, Pavillon T. Hospices Civils de Lyon
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Lyon, Rhone, France, 69003
- Service de gériatrie aigue de l'hôpital Edouard Herriot. Hospices Civils de Lyon
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Pierre-Bénite, Rhone, France, 69495
- Service de gériatrie aigue de l'hôpital Lyon Sud. Hospices Civils de Lyon
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Villeurbanne, Rhone, France, 69100
- Service de gériatrie aigue de l'hôpital des Charpennes. Hospices Civils de Lyon
-
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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:
- Patient over 70 years of age.
- Patient hospitalized in short geriatric units in University Hospital of Lyon.
- Patient diagnosed with COVID-19 (positive Polymerase Chain Reaction or a high presumption of COVID-19 based on clinical and/or scannographic evidence).
- Patient Informed and non-opposed to the research (Patient informed of the study by his medical doctor during hospitalization or by post, thanks to a generic information sheet dedicated to COVID-19 researches).
Exclusion Criteria:
- Patient opposed to the research.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Elder patients hospitalized for COVID-19 in geriatric short stay units.
All patients over 70 years of age, with a positive Polymerase Chain Reaction or a high presumption of COVID-19, hospitalized in short geriatric units in University Hospital of Lyon, who agree with retrospective collection of their clinical datas.
|
Retrospective clinical data collection, at time of infection and 10 days later.
Correlation between mortality and gravity.
Identification of predictive mortality factors such as frailty, preexisting comorbidities, complications and treatments.
Description of medical prescription evolutions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
In hospital mortality rate.
Time Frame: During patient hospitalization, an average of 10 days.
|
Observed mortality rate will be presented with its 95% confidence interval.
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During patient hospitalization, an average of 10 days.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ANTICIPATED)
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
- AGORA n°36
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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