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Pre-malignant States to Hematologic Malignancies in Firefighters

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Enrolling

Conditions

Multiple Myeloma
Clonal Hematopoiesis of Indeterminate Potential
Plasma Cell Disorder
Monoclonal Gammopathy
Leukemia
Non Hodgkin Lymphoma

Treatments

Other: Monoclonal Gammopathy
Other: Complete Blood Count with differential (CBC w/ diff)
Other: Clonal hematopoiesis (CHIP)

Study type

Observational

Funder types

Other

Identifiers

NCT06870760
LCI-LEU-FF-CHIP-001 (Other Identifier)
IRB00124175

Details and patient eligibility

About

The purpose of the study is to evaluate if firefighter exposure to hazardous compounds will increase the incidence of premalignant hematological states which subsequently increases the risk of the development of hematologic malignancies, and potentially other pathophysiological consequences.

Full description

Firefighters from the Charlotte Fire Department, ages 40-49 and with at least 5 years on the job experience will be offered consent for this study. Consented and eligible participants will have labs collected at the Baseline visit to evaluate for CHIP and monoclonal gammopathy. Buccal swabs (also collected at Baseline) and any remaining blood from the Baseline labs will be collected from participants who consent to collection and banking of their samples for future research. Participants will also complete the Firefighter History Assessment at Baseline.

If clonal hematopoiesis (CHIP) results are interpreted by the investigator as abnormal, the participant will be given a clinical referral if indicated for discussion of diagnosis, potential further diagnostic tests, and implications per standard CHIP management guidelines. If monoclonal gammopathy or other (concerning) abnormality of the complete blood count is detected, the participant will be provided a referral for a clinic visit for diagnostic assessments and followed up per standard of care.

If the participant proceeds with the referral and diagnostic work-up, the final diagnosis (if any) resulting from the initial diagnostic assessment(s) will be collected

Enrollment

300 estimated patients

Sex

All

Ages

40 to 49 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Written informed consent and HIPAA authorization for release of personal health information.
  2. Age ≥ 40-49 years at the time of consent (self-reported)
  3. Ability of the participant to understand and comply with study procedures for the entire length of the study
  4. Currently employed by Charlotte Fire Department (CFD) with at least 5 years on-the -job experience (self-reported)

Exclusion criteria

Anyone with a current diagnosis of a hematologic malignancy will be excluded.

Trial design

300 participants in 1 patient group

Firefighter
Description:
Participants employed by the Charlotte Fire Department (CFD) with at least 5 years of on-the-job experience between the ages of 40 and 49
Treatment:
Other: Clonal hematopoiesis (CHIP)
Other: Complete Blood Count with differential (CBC w/ diff)
Other: Monoclonal Gammopathy

Trial contacts and locations

1

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Central trial contact

Megan Lattanze

Data sourced from clinicaltrials.gov

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