- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04664296
COVID-19 - SARS-CoV-2 Community Contamination in Children and Adults (Dyn3CEA_Nosocor)
Epidemiology of CoV-2 SARS Infections: Dynamics of Community Contamination in Children and Adults
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Rhone
-
Lyon, Rhone, France, 69003
- Service de réanimation pédiatrique
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Hospital-based population of children and adults:
- Hospitalized children, 0 to 17 years of age, 25 subjects, consecutive sample survey
- Hospitalized adults, 18 years and above, 50 matched subjects
Description
Inclusion Criteria:
- Children after hospitalized in Hospices Civils de Lyon with Polymerase Chain Reaction (PCR) positive SARS-CoV2,
Adults hospitalized in Hospices Civils de Lyon and included in the NOSO-COR study with matching criteria described below.
- Matching will be performed on family age characteristics and on the period of contamination included in the containment period to minimize bias, and if possible frequency matching according to admission in Intensive Care Unit ICU/Pediatric Intensive Care Unit (PICU), and to family structure (n of children / n of adults in the family).
Exclusion Criteria:
- Any patient suspected of nosocomial infection.
- Any patient death during the Covid-19 infection.
- Any adult patient without children living home.
- Opposition to participate.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Children
Hospitalized children, 0 to 17 years of age, 25 subjects, consecutive sample survey
|
Review of medical patient file, including patient tracing, brief summary of the disease course, barrier gestures, social distancing.
|
|
Adults
Hospitalized adults, 18 years and above, 50 matched subjects
|
less than 15 minutes phone call
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of possible contaminants, adults, adolescents and children with Covid-19
Time Frame: at inclusion
|
To describe the age category of the 1st possible contaminant in the index case to show the preponderance of possible adult and adolescent contaminants in the SARS-Cov-2 contamination. Percentage of possible contaminants, adults, adolescents and children, in matched children and adults with Covid-19. |
at inclusion
|
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
- 69HCL20_1100
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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