Genomics and COVID-19 Vaccine Adverse Events

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age5-99
SponsorUniversity of British Columbia

About this trial

Vaccines routinely used are extremely safe; however, severe adverse events to vaccines do occur. As vaccination against COVID-19 has begun, adverse events to the vaccine, particularly Guillain-Barré syndrome (GBS), vaccine-induced immune thrombotic thrombocytopenia (VITT)/thrombosis with thrombocytopenia syndrome (TTS), and myocarditis/pericarditis, after COVID-19 vaccination have been reported worldwide.

Study hypothesis: there are genetic factors that contribute to increased risks of particular COVID-19 vaccine-induced adverse events.

The objective of the study is to determine if there are specific genetic factors strongly associated with each of the COVID-19 vaccine-induced adverse events (i.e., GBS, VITT/TTS, and myocarditis/pericarditis).

Eligibility criteria

Qualifiers

Case: Any patient who received COVID-19 vaccines and developed GBS, VITT/TTS, or myocarditis/pericarditis after vaccination

Control: Any participant who received COVID-19 vaccines and does not experience GBS, VITT/TTS, or myocarditis/pericarditis.

Disqualifiers

Individuals who have not received a COVID-19 vaccine

Individuals who are unable to provide informed consent

Trial design

Treatments tested in this trial

  • COVID-19 vaccines

Treatment groups

6,325 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of British Columbia

Lead sponsor

Centers for Disease Control and Prevention

Collaborator