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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04664296
Other study ID # 69HCL20_1100
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 21, 2020
Est. completion date March 23, 2021

Study information

Verified date April 2021
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Unlike other respiratory viruses such as influenza and Respiratory Syncytial Virus (RSV) where the child is the essential reservoir and central vector of intrafamilial contamination, the child is likely to be a small player in the transmission of Severe Acute Respiratory Syndrome CoronaVirus 2 (SRAS-CoV2) infection. This study aims to describe the age category of the first contact, within 14 days before the appearance of the first symptoms of the index case in order to describe the age categories of this first contaminant, globally, in the group of children and finally in the group of adults. This work is intended to provide food for discussion and to justify the distancing and containment measures imposed on children when their isolation has a deleterious impact that has now been established for some children.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date March 23, 2021
Est. primary completion date March 23, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Children after hospitalized in Hospices Civils de Lyon with Polymerase Chain Reaction (PCR) positive SARS-CoV2, 2. 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: 1. Any patient suspected of nosocomial infection. 2. Any patient death during the Covid-19 infection. 3. Any adult patient without children living home. 4. Opposition to participate.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Review of medical patient file
Review of medical patient file, including patient tracing, brief summary of the disease course, barrier gestures, social distancing.
Phone call interview
less than 15 minutes phone call

Locations

Country Name City State
France Service de Reanimation Pediatrique Lyon Rhone

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of possible contaminants, adults, adolescents and children with Covid-19 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
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