Project PHOENIX: Molecular Signatures of Burn Pit Exposure

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCreative Medical Technology Holdings Inc

About this trial

Project PHOENIX is an observational clinical research study designed to characterize molecular, genomic, cellular, and functional features in blood specimens from former U.S. Service Members with prior burn pit exposure and from matched unexposed controls. Participants will complete screening, informed consent, health and exposure questionnaires, and a one-time blood collection. Blood-derived specimens may undergo genomic, epigenomic, transcriptomic, proteomic, metabolomic, immunophenotyping, and cellular functional analyses. Participants may also agree to optional future re-contact for health updates and possible repeat blood collection. The goal is to identify biologic signatures associated with prior deployment-related burn pit exposure and to support future biomarker discovery and translational research in veteran health.

Eligibility criteria

Qualifiers

Age 18 years or older at the time of consent

Former or current U.S. Service Member, including Active Duty, Reserve, National Guard, or Veteran status

For exposed cohort: prior deployment to a location with known burn pit operations, based on participant report and available confirmation when feasible

For control cohort: no known deployment to burn pit locations

Disqualifiers

Active serious illness or infection that, in the investigator's judgment, would compromise participation or specimen integrity

Receipt of systemic chemotherapy, immunotherapy, or radiation therapy within the past 6 months

High-dose systemic immunosuppression, defined as more than 20 mg prednisone equivalent daily for more than 14 days within the past 3 months

Pregnant or currently breast-feeding

Trial design

Treatments tested in this trial

  • Prior Burn Pit Exposure
  • No Known Burn Pit Exposure

Treatment groups

1,000 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators