Clinical trial
TG Gene Mutations and Congenital Hypothyroidism
NCT00493103 · University of Sao Paulo, Other · Completed
Key facts
| NCT number | NCT00493103 |
|---|---|
| Title | TG Gene Mutations and Congenital Hypothyroidism |
| Official title | Congenital Hypothyroidism Due to Thyroglobulin Mutations in an Inbred Brazilian Family: A Novel Compound Heterozygous Constellation and Intronic Mutation Related to Fetal Goiter. |
| Lead sponsor | University of Sao Paulo, Other |
| Collaborators | Fundação de Amparo à Pesquisa do Estado de São Paulo |
| Status | Completed |
| Study type | Observational |
| Conditions | Congenital Hypothyroidism |
| Start date | Jul 1, 2003 |
| Completion | Jun 1, 2007 |
| First posted | Jun 27, 2007 |
| Last update posted | Jun 27, 2007 |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: