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90-Day Cobalt Supplementation Study to Investigate the Cobalt Body Burden in Ten Healthy Adult Volunteers

NCT01990794 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 13

Last updated 2014-10-06

Study results available
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Summary

The purpose of this study is to investigate steady-state cobalt levels following dietary supplementation for 90 days with 1 mg cobalt/day (as cobalt chloride in solution) in healthy adult volunteers.

Conditions

  • Cobalt Biokinetics
  • Safety of Cobalt Dietary Supplementation

Sponsors & Collaborators

  • DePuy Orthopaedics

    collaborator INDUSTRY

  • Cardno ChemRisk

    lead OTHER

Principal Investigators

  • David Galbraith, MD · Cardno ChemRisk

  • David Galbraith, MD · Cardno ChemRisk

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2013-03-31
Completion
2013-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01990794 on ClinicalTrials.gov