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Assessment of Myocarditis After Replication-Deficient Smallpox Immunization
Sponsor: Womack Army Medical Center
Summary
This is a prospective observational phase IV study of a novel, replication-deficient smallpox vaccine that has been recently been approved by FDA. The purpose of this study is to determine if there are any abnormalities detected by electrocardiographic testing and/or blood tests within 35 days of receiving the second dose of smallpox vaccine either alone or co-administered with other vaccines that may/may not be suggestive of myopericarditis.
Official title: Prospective Assessment of Myocarditis After Replication-Deficient Smallpox Immunization
Key Details
Gender
All
Age Range
18 Years - 45 Years
Study Type
OBSERVATIONAL
Enrollment
2350
Start Date
2029-03
Completion Date
2033-10
Last Updated
2023-12-14
Healthy Volunteers
Yes
Conditions
Interventions
JYNNEOS
smallpox vaccine