Clinical Trials Directory

Trials / Completed

CompletedNCT00271427

Selenium Treatment in Autoimmune Thyroiditis (AIT)

Selenium Treatment in Autoimmune Thyroiditis: Long Term Follow-Up With Variable Doses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (planned)
Sponsor
Ege University · Academic / Other
Sex
Female
Age
15 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Selenium suppresses autoimmune destruction of thyrocytes and decreases titers of serum TPOAb in AIT patients. Older 4 clinical trials approved the efficacy of the daily dose of 200micg. It's believed that Se saturates the deficient stores of GPX so GPX saves the thyrocytes against to oxidative stresses. Although less than 70 micg/d is sufficient to maximize GPX activity, none of the authors tested the doses less than 200 micg/d. Our hypothesis was that If 100 micg/d can not suppress the TPOAb titers,it means autoimmune destruction can not be blocked by saturation of deficient stores of GPX solely and the mechanism of action requires more than repletion of deficient stores. It's important not only to estimate the optimal dose but to understand the mechanism of action. High dose therapy may also suppress TPOAb levels in Se-non-deficient AIT patients, if it is so, Se therapy may becomes the solely treatment modality which can suppress the autoimmunity in more than 400 million AIT patients. Because there've been no way to suppress autoimmune war and replacement of LT4 had been the only treatment modality for palliation. An other independent part of the study is to test the effect of Se in adolescent AIT patients.

Conditions

Interventions

TypeNameDescription
DRUGL-Selenomethionine

Timeline

Start date
2004-12-01
Completion
2005-08-01
First posted
2006-01-02
Last updated
2006-08-23

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT00271427. Inclusion in this directory is not an endorsement.