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NCT05656664
Mitigation Efforts in Arsenic Exposure With Folic Acid Supplementation
Conditions: Arsenic and/or Arsenic Compound Adverse Reaction
Sex: All
Ages: 18 Years – 89 Years
Healthy volunteers: 1
Phase: NA
Enrollment: 100
Sponsor: University of Alabama at Birmingham
Location: United States
Summary
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.
Eligibility Criteria
Inclusion Criteria:≥18 years of ageResident of the superfund siteClinically stable with no significant changes in general health status in the past 4 weeks prior to screening as assessed by the investigatorProvide written informed consentExclusion Criteria:PregnancyOngoing folic acid nutritional supplementationMethotrexate useMegaloblastic anemiaAlcoholic liver diseaseMalabsorptive syndromes - celiac disease, inflammatory bowel disease
Source: ClinicalTrials.gov (NCT05656664). StuddyBuddy aggregates publicly available trial information.
