Trials / Completed
CompletedNCT06588530
PFAS Exposure and Immune Response to Vaccination in Adults
Effects of Exposure to Per- and Polyfluoroalkyl Substances (PFAS) on Innate and Adaptive Immune Responses to Tetanus-diphtheria (Td) Vaccination Among Adults in a Community-based Panel Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Rutgers, The State University of New Jersey · Academic / Other
- Sex
- All
- Age
- 18 Years – 89 Years
- Healthy volunteers
- Accepted
Summary
This clinical trial aims to investigate how exposure to Perfluorononanoic acid (PFNA), a type of per- and polyfluoroalkyl substance (PFAS), affects the immune response to the standard tetanus and diphtheria (Td) vaccine. The study focuses on participants from a community with known prior PFNA exposure through contaminated drinking water. The main question it aims to answer is: * Does exposure to PFNA weaken the body's initial immune response, leading to lower levels of protective antibodies after vaccination? Participants will: * Receive Tetanus and Diphtheria (Td) booster vaccination * Visit the study office 7 times over a 30-day period * Have blood and saliva collected at each study visit
Conditions
- Innate Inflammatory Response
- Vaccination
- Diphtheria
- Tetanus
- Environmental Exposure
- Vaccine
- Antibodies
- Adult
- Immunity
- Pollution; Exposure
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | TENIVAC | TENIVAC (Tetanus and Diphtheria Toxoids Adsorbed) is an active immunization for the prevention of tetanus and diphtheria in persons 7 years of age and older. |
Timeline
- Start date
- 2024-11-04
- Primary completion
- 2025-01-08
- Completion
- 2025-01-08
- First posted
- 2024-09-19
- Last updated
- 2025-12-30
- Results posted
- 2025-12-30
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06588530. Inclusion in this directory is not an endorsement.