TG Gene Mutations and Congenital Hypothyroidism

NCT00493103 · Status: COMPLETED · Type: OBSERVATIONAL

Last updated 2007-06-27

No results posted yet for this study

Summary

The aim of this study was to identify mutations in the thyroglobulin gene that might be present in patients with fetal goiter and congenital goiter hypothyroidism.

Conditions

  • Congenital Hypothyroidism

Sponsors & Collaborators

  • Fundação de Amparo à Pesquisa do Estado de São Paulo

    collaborator OTHER_GOV
  • University of Sao Paulo

    lead OTHER

Principal Investigators

  • Viviane Pardo · University of Sao Paulo

  • Geraldo Medeiros-Neto · University of Sao Paulo

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-07-31
Completion
2007-06-30

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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 NCT00493103 on ClinicalTrials.gov