Understanding Immunity to the COVID-19 Vaccines
Sponsor
Stanford University (Other)
Overall Status
Completed
CT.gov ID
NCT04664309
Collaborator
National Institutes of Health (NIH) (NIH)
43
1
9.4
4.6
Study Details
Study Description
Brief Summary
The purpose of this study is to test over time immunity to the COVID-19 vaccines. Adults who are receiving COVID-19 vaccines will be invited to participate.
Study Design
Study Type:
Observational
Actual Enrollment
:
43 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Understanding Immunity to the COVID-19 Vaccines
Actual Study Start Date
:
Mar 26, 2021
Actual Primary Completion Date
:
Jan 6, 2022
Actual Study Completion Date
:
Jan 6, 2022
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Participants Adults who are receiving a COVID-19 vaccine |
Other: No intervention
No intervention
|
Outcome Measures
Primary Outcome Measures
- Percentage of participants with immunity to COVID-19 vaccines over time [1 year]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- Adults who are receiving a COVID-19 vaccine
Exclusion Criteria:
- Patients with special risks attendant to venipuncture
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Stanford University, Hospital, and Clinics | Stanford | California | United States | 94305 |
Sponsors and Collaborators
- Stanford University
- National Institutes of Health (NIH)
Investigators
- Principal Investigator: Kari Nadeau, MD, PhD, Stanford University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Kari Christine Nadeau, MD, PhD,
Professor of Medicine,
Stanford University
ClinicalTrials.gov Identifier:
NCT04664309
Other Study ID Numbers:
- IRB-60171
First Posted:
Dec 11, 2020
Last Update Posted:
Feb 28, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: