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NCT05656664

Mitigation Efforts in Arsenic Exposure With Folic Acid Supplementation

ENROLLING BY INVITATION NA Last updated 17 July 2025
What this trial tests

NA trial testing Folic Acid in Arsenic and/or Arsenic Compound Adverse Reaction in 100 participants. Enrolling by invitation.

Timeline
14 September 2023
Primary endpoint
31 December 2025
31 December 2026

Quick facts

Lead sponsorUniversity of Alabama at Birmingham
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment100
Start date14 September 2023
Primary completion31 December 2025
Estimated completion31 December 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Alabama at Birmingham

Who can join

Adults 18 to 89, any sex, with Arsenic and/or Arsenic Compound Adverse Reaction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Folic Acid

Trials testing the same drug.

Other University of Alabama at Birmingham trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05656664.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing