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The effect of Selenium and Vitamin C for treatment of Hashimoto thyroiditis

Effect of treatment with Selenium and Vitamin C in comparison to placebo on serum level of anti-thyroid peroxidase antibody in patients with Hashimoto, thyroiditis, a clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013092014717N1
Enrollment
84
Registered
2015-05-13
Start date
2012-09-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hashimoto thyroiditis. Autoimmune thyroiditis

Interventions

Intervention 1: The first intervention group will receive Selenium 200 micrograms tablet daily by mouth, for 3 to 6 months. Selenium tablets will be prepared from Sodium Selenate from Merck company by
Treatment - Drugs
The first intervention group will receive Selenium 200 micrograms tablet daily by mouth, for 3 to 6 months. Selenium tablets will be prepared from Sodium Selenate from Merck company by Shiraz school o
The second intervention group will receive 500 milligrams tablet of Vitamin C daily, by mouth, for 3 to 6 months. Vitamin C tablets will be prepared by Avicenna company
The control group will receive one tablet of placebo which will contain starch and will be similar to the real drugs. The placebo tablets will be prepared by Shiraz school of pharmacy

Sponsors

Research Vice-Chancellor of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age, 15 years old or more; anti-thyroid peroxidase antibody titer 200 units per liter or more. Exclusion criteria: pregnant women; previous history of thyroid disorders; previous history of hypothalamo-hypophyseal disorders; presence of nonthyroidal disorders (such as renal; hepatic; cardiovascular disorders; diabetes mellitus; infectious diseases; renal stone; etc) ; consumption of drugs with effect on thyroid hormones metabolism; consumption of sex hormones; glucocorticoids; vitamins or supplements

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Titer of anti-thyroid peroxidase antibody. Timepoint: Before and after 3 to 6 months of treatment. Method of measurement: Measurement of anti-thyroid peroxidase antibody titer in serum by radioimmunoassay method.

Secondary

MeasureTime frame
Thyroid function test including: thyroxine, thriiodothyronine, and thyroid stimulating hormone levels. Timepoint: Before treatment and after completion of treatment course. Method of measurement: Measurement of serum levels of hormones by immunoradiometric assay method.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Fariba Karimi

Shiraz University of Medical Sciences

karimif@sums.ac.ir+98 71 3647 4316

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026