TG Gene Mutations and Congenital Hypothyroidism
Congenital Hypothyroidism Due to Thyroglobulin Mutations in an Inbred Brazilian Family: A Novel Compound Heterozygous Constellation and Intronic Mutation Related to Fetal Goiter.
1 other identifier
observational
N/A
0 countries
N/A
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Jul 2003
Longer than P75 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2003
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2007
CompletedFirst Submitted
Initial submission to the registry
June 25, 2007
CompletedFirst Posted
Study publicly available on registry
June 27, 2007
CompletedJune 27, 2007
June 1, 2007
June 25, 2007
June 25, 2007
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Patients with congenital hypothyroidism due to thyroglobulin defective synthesis.
You may not qualify if:
- Patients with another disease.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Viviane Pardo
University of Sao Paulo
- STUDY DIRECTOR
Geraldo Medeiros-Neto
University of Sao Paulo
Study Design
- Study Type
- observational
- Time Perspective
- OTHER
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
June 25, 2007
First Posted
June 27, 2007
Study Start
July 1, 2003
Study Completion
June 1, 2007
Last Updated
June 27, 2007
Record last verified: 2007-06