National Vaccine Adverse Event Reporting Survey and Etiology (NVAERS)

Neuroganics

Status: Unknown

Conditions: Guillain-Barré; Neuritis; Thrombocytopenia; GWAS; Vaccine Reaction; Genetic Sequencing; COVID-19; Vaccine Adverse Reaction; Blood Clot; Corona Virus Infection; Influenza; Vaccine or Biological Substance, Unspecified Causing Adverse Effects in Therapeutic Use; Vasculitis

Treatments: Biological: vaccinated

Study type: Observational

Funder types: Industry; Other

Identifiers

NCT05095844

NVAERS_1121

Details and patient eligibility

About

If your serious vaccine-induced adverse event has been entered in the CDC Vaccine Adverse Event Reporting System (VAERS) we are interested in enrolling you for this study in order to log your symptoms.

The primary goal of this study is to create a national database and gather vaccine-associated serious adverse events/injury data from newly vaccinated individuals in the US in order to identify the possible underlying causal relationships and plausible underlying biological mechanisms. The project aims to identify the genetic determinants of vaccine-induced adverse response by studying host genetics. We plan to use whole genome sequencing to identify single nucleotide polymorphisms associated with cardiovascular, neurological, gastrointestinal, musculoskeletal and immunological symptoms induced by vaccine administration.

The secondary goal is to establish criteria that enable classification of vaccine-induced adverse events/injuries compare data from our database with the official Vaccine Injury Table National Vaccine Injury Compensation Program on or after March 21, 2017.

The tertiary goal is to establish a database to gather detailed long-term adverse reaction data from subjects enrolled in FDA Emergency Use Authorized vaccine clinical trials.

Full description

Vaccinations are typically administered to healthy persons and often are mandated by states or federal authorities as a condition for school attendance or military service in order to prevent the spread of infectious diseases. Because vaccines are either mandated or recommended for vulnerable groups, such as children or the elderly, vaccines are often held to a higher standard of safety by the FDA than other medical products.

Due to the vast numbers of vaccine doses administered in the US there is a need to gather quality information on serious vaccine-associated adverse events leading to serious injury. Vaccine-induced adverse events are typically reported in the CDC Vaccine Adverse Event Reporting System (VAERS) database, which contains information on unverified reports of adverse events (illnesses, health problems and/or symptoms) following immunization with US-licensed vaccines. Reports are accepted from anyone and can be submitted electronically at www.vaers.hhs.gov.

The primary goal for this observational study is to establish an independent national database to classify vaccine-associated serious adverse events/injury data from vaccinated individuals. The plan is to gather survey data and health information from newly vaccinated individuals who have experienced serious adverse effects in order to help understand the possible causal relationships and plausible biological mechanisms underlying serious adverse events/injuries. The project aims to identify the genetic determinants of vaccine-induced adverse response by studying host genetics. We plan to use Nebula Genomics platform for whole genome sequencing to identify single nucleotide polymorphisms associated with cardiovascular, neurological, gastrointestinal, musculoskeletal and immunological symptoms induced by vaccine administration.

The secondary goal is to gather medical history and survey data from recently vaccinated individuals in order to develop a vaccine-injury risk assessment tool which may be used to predict individual vulnerability to vaccine adverse events/injury.

The tertiary goal is to establish a database to gather detailed long-term adverse reaction data from subjects enrolled in FDA Emergency Use Authorized vaccine clinical trials.

Enrollment: 100,000 estimated patients

Sex: All

Ages: 5 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Individuals who have received at least one vaccine dose of ANY of the following vaccines (below) and experienced adverse reaction within 60 days of vaccine administration:

1. Pfizer-BioNTech COVID-19 Vaccine
2. Moderna COVID-19 Vaccine
3. J&J/Janssen COVID-19 Vaccine
4. Diphtheria (e.g., DTP, DTaP, Tdap, DT, Td, TT)
5. Haemophilus influenza type b polysaccharide conjugate vaccines (e.g., Hib)
6. Hepatitis A (e.g., HAV)
7. Hepatitis B (e.g., HBV)
8. Human papillomavirus (e.g., HPV)
9. Seasonal influenza (e.g., Flu)
10. Measles (e.g., MMR)
11. Mumps (e.g., MMR, MR, M)
12. Meningococcal (e.g., MCV4, MPSV4, MenB-FHbp, MenB-4C)
13. Pertussis (e.g., DTP, DTaP, Tdap)
14. Pneumococcal conjugate (e.g., PCV)
15. Polio (e.g., OPV or IPV)
16. Rotavirus (e.g., RV)
17. Rubella (e.g., MMR, MR, R)
18. Tetanus (e.g., Td)
19. Varicella (e.g., VAR).

Exclusion criteria

1. Non citizens or permanent residents of the US

2. Individuals who have not received at least one vaccine dose in the past 3 years.

3. Individuals whose vaccine was administered more than 60 days before symptoms of the serious adverse event.

Trial design

100,000 participants in 1 patient group

Vaccinated

Description:

All individuals who have received a vaccine dose.

Treatment:

Biological: vaccinated