Mitigation Efforts in Arsenic Exposure With Folic Acid Supplementation

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
University of Alabama at Birmingham
Study ID
NCT05656664
Status
Enrolling By Invitation

Conditions

  • Arsenic and/or Arsenic Compound Adverse Reaction

Eligibility Criteria

Sex
ALL
Age
18 Years - 89 Years
Healthy Volunteers
Accepted

Interventions

  • Folic Acid — DIETARY_SUPPLEMENT
    Folic acid supplementation to assess for increased arsenic metabolite excretion
  • Placebo — OTHER
    Placebo group to assess arsenic metabolite excretion

Study Details

The purpose of this study is to evaluate the effects on folic acid supplementation in a population living in an environment with chronic arsenic exposure in Birmingham, Alabama.

Key Dates

Start date
Sep 14, 2023
Status verified
Mar 2026
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
100 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • Placebo Comparator: Placebo
    Placebo daily 12 weeks
  • Experimental: Folic Acid
    Folic acid 800 ug/day 12 weeks

Primary Outcome Measure

Measurement of urine and blood arsenic metabolites [ Time Frame: 12 weeks ]

Locations (1)

FacilityCityStateZIPSite coordinators
UAB Lung Health CenterBirminghamAlabama35205-

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