Clinical Trials Directory

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

Interventions

TypeNameDescription
BIOLOGICALTENIVACTENIVAC (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

Source: ClinicalTrials.gov record NCT06588530. Inclusion in this directory is not an endorsement.