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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04408014
Other study ID # COVID-19-Epi-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2020
Est. completion date July 30, 2020

Study information

Verified date February 2024
Source Butantan Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Seroepidemiological Study of SARS-CoV-2 Infection in Population Subgroups in the State of São Paulo


Description:

This is a cross-sectional study to estimate the prevalence of antibodies against SARS-CoV-2 is different population subgroups in the State of São Paulo


Recruitment information / eligibility

Status Completed
Enrollment 18901
Est. completion date July 30, 2020
Est. primary completion date July 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Months to 100 Years
Eligibility Inclusion Criteria: - All potential volunteers invited to participate in the study. Exclusion Criteria: - All potential eligible participants, but who do not show interest in participating in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Serological test
IgM and IgG for SARS-CoV-2
Nasopharyngeal Swab
PCR for SARS-CoV-2
Oropharyngeal Swab
PCR for SARS-CoV-2

Locations

Country Name City State
Brazil Avenida Vital Brasil 1500 Sao Paulo

Sponsors (1)

Lead Sponsor Collaborator
Butantan Institute

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of antibodies against SARS-CoV-2 through serological testing IgM and IgG antibodies against SARS-CoV-2 1 month
Primary Frequency of participants with a positive RT-PCR test result for SARS-CoV-2 Positive RT-PCR test result for SARS-CoV-2 1 month
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