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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04670003
Other study ID # WP-2020-05
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2, 2021
Est. completion date March 30, 2021

Study information

Verified date December 2020
Source Weprom
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

A coronavirus pandemic began on 12/31/2019 with a first Chinese patient. As of 04/04/2020, the epidemic affects more than 190 countries with more than 50 million official contaminations and 1,251,000 deaths. (Univ J Hopkins). This virus causes a pathology ranging from simple flu-like symptoms in 80% of cases to acute respiratory distress syndromes requiring intensive care in 5% of cases and a death rate of 1.4 to 4% of cases. Viral contamination is airborne and fecal A first epidemic wave crossed France in March / April 2020 then a second in October / November with a source of contamination which began in mid-August 2020. The sources of propagation are not well known (what places, what times, what contacts…? ) In the context of the health crisis linked to the coronavirus, knowledge of the sources of propagation of this 2nd wave is an important issue to guide end of lockdown and second lockdown policies.


Recruitment information / eligibility

Status Completed
Enrollment 4975
Est. completion date March 30, 2021
Est. primary completion date March 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - users of the application - not having objected to the use of their data Exclusion criteria: - user who does not have a complete questionnaire

Study Design


Related Conditions & MeSH terms


Intervention

Other:
users
Data of users of the web-application

Locations

Country Name City State
France Institut Interrégional de Cancérologie Le Mans

Sponsors (2)

Lead Sponsor Collaborator
Weprom Kelindi

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Description of the methods of contamination of patients Data and symptomes collected by the web applications self-questionnaire (patient reported outcome) 2 months
Secondary Evaluation in time of the spread of the virus during the 2nd epidemic wave. Data and symptomes collected by the web applications self-questionnaire (patient reported outcome) 2 months
Secondary Evaluation in space of the spread of the virus during the 2nd epidemic wave. Data and symptomes collected by the web applications self-questionnaire according to ZIP code (patient reported outcome) 2 months
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