Vaccine Observation to Include All Communities for Equitable Science
NCT ID: NCT04770649
Last Updated: 2024-04-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
15 participants
OBSERVATIONAL
2021-04-01
2022-12-31
Brief Summary
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Subjects who meet the entry criteria will provide two samples each of blood, one prior to and one following vaccine administration. Follow-up questionnaires will be sent at 3, 6, 9, and 12 months to determine if participants have contracted COVID-19 or have experienced any adverse effects of the vaccine. Nasal swab samples will also be collected from participants that have contracted COVID-19. The samples will be analyzed to determine the impact of gut microbiome composition and function on the immune system and vaccine efficacy.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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COVID-19 vaccine recipients
Subjects who have an appointment to receive a COVID-19 vaccine, and are able to provide samples prior to and after their first vaccine dose.
COVID-19 vaccine
Any vaccine for COVID-19
Interventions
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COVID-19 vaccine
Any vaccine for COVID-19
Eligibility Criteria
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Inclusion Criteria
* Subjects who are able to provide written informed consent.
Exclusion Criteria
* Subjects without the mental capacity to complete either a written or online questionnaire, alone or with assistance, or make sound decisions
* Women who are pregnant, plan on becoming pregnant, or are nursing.
18 Years
ALL
Yes
Sponsors
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Persephone Biosciences
INDUSTRY
Responsible Party
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Locations
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Persephone Biosciences, Inc.
San Diego, California, United States
Countries
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Other Identifiers
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PB-2021-01
Identifier Type: -
Identifier Source: org_study_id
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