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Clinical Trial Summary

The purpose of this experiment is to compared the changes of thyroid function, anti-thyroid peroxidase antibody, anti-thyroglobulin antibody, thyroid magnetic resonance T1-mapping and various metabolic indexes from baseline to the end of treatment (after the thyroid function had been normal for more than three months)


Clinical Trial Description

In patients with autoimmune thyroiditis with mild subclinical hypothyroidism, the study period will include a screening period of not more than 30 days, and a 12-week treatment period compared to baseline. At completion of treatment, Thyroid Stimulating Hormone(TSH), free thyroxine (FT4),free thyroxine (FT3) will be included. The changes of anti-thyroglobulin antibody, anti-thyroglobulin antibody, T1-mapping and metabolic indexes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04953195
Study type Interventional
Source Beijing Chao Yang Hospital
Contact Jia Liu, MD
Phone 861085231710
Email liujia0116@126.com
Status Recruiting
Phase Phase 4
Start date January 1, 2019
Completion date October 30, 2021