Thyroid Dysfunction in Head and Neck Surgery Patients

NCT00592514 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 14

Last updated 2011-09-02

No results posted yet for this study

Summary

Specific Aim I: Determine absorption of iodine after oropharyngeal application of povidone-iodine 10% solution when used in head and neck surgery involving the upper aero-digestive tract.

Specific Aim II: Measurement of iodine induced changes in thyroid function.

Conditions

  • Thyroid Dysfunction

Sponsors & Collaborators

  • University of Arkansas

    lead OTHER

Principal Investigators

  • James Suen, MD · University of Arkansas

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2008-07-31
Completion
2008-07-31

Countries

  • United States

Study Locations

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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 NCT00592514 on ClinicalTrials.gov