Sars-CoV-2 Infection Clinical Trial
Official title:
Effectiveness Evaluation of the Sinopharm Vaccine in the Dondo District in Mozambique
Three complementary activities will be implemented:1) Baseline and repeat census of the catchment population; described in a separate protocol (IVI-ECOVA-03-WS1); 2) Enhanced surveillance for COVID-19 disease, and 3) AEFI-enhanced surveillance. The mass vaccination campaign will be conducted by the Government and is not part of this protocol.
Status | Recruiting |
Enrollment | 3000 |
Est. completion date | August 30, 2024 |
Est. primary completion date | February 28, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. They resided in the study area at the time of mass immunization with the Sinopharm vaccine; and 2. They are at least 18 years of age during first round of mass vaccination. 3. Their onset of symptoms was <10 days prior to testing. 4. For each selected PCR test-positive case, we will select up to 3 test-negative controls from generally eligible subjects, matched to each case by age on the date of testing, sex, and calendar date of testing + 3 days. Exclusion Criteria: 1. We will exclude subjects for selection as controls if they have had a positive test result within the following 21 days 2. Any Participant not matching the inclusion criteria mentioned above. |
Country | Name | City | State |
---|---|---|---|
Mozambique | Dondo Health Facility | Dondo |
Lead Sponsor | Collaborator |
---|---|
International Vaccine Institute | Harvard University, Heidelberg University, Instituto Nacional de Saúde (INS), Mozambique, International Centre for Diarrhoeal Disease Research, Bangladesh, The Coalition for Epidemic Preparedness Innovations (CEPI), University of Antananarivo |
Mozambique,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Protection conferred by two completed doses of Sinopharm vaccine against confirmed COVID-19 disease | Protection conferred by two completed doses of Sinopharm vaccine against RT-PCR-confirmed COVID-19 disease measured as the reduction in risk in adults who received two completed doses of the vaccine compared to those who are not vaccinated. | 2 years | |
Secondary | Evaluate the effectiveness of two completed doses of the Sinopharm vaccine against severe SARS-CoV-2 infection | Evaluate the effectiveness of two completed doses of the Sinopharm vaccine against RT-PCR confirmed severe SARS-CoV-2 infection | 2 years |
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