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Selenium in Mild Thyroid Eye Disease in North America

Selenium - ITEDS: A North American Study

Status
Withdrawn
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02112643
Acronym
S-ITEDS
Enrollment
0
Registered
2014-04-14
Start date
2015-10-31
Completion date
2016-11-16
Last updated
2021-08-18

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

Conditions

Thyroid Associated Ophthalmopathies

Keywords

Thyroid eye disease, Thyroid orbitopathy, Graves' orbitopathy, Graves' ophthalmopathy

Brief summary

The purpose of this study is to determine whether sodium selenite is helpful in the treatment of mild thyroid eye disease in North America.

Detailed description

Thyroid eye disease (TED) is a disease in which the soft tissues surrounding the eye can become inflamed, scarred, and at times permanently damaged in an autoimmune reaction highly associated with abnormal thyroid hormone levels. Some patients have much more severe TED than others, but overall, most patients reach a point with relatively stable TED after 1 to 2 years. A recent European study showed that oral selenium, a trace mineral involved in anti-oxidation and immune regulation, could actually alter the course of mild TED, lessening its signs and symptoms and even improving the quality of life of those who took it. The investigators would like to perform a sister study throughout North America. In this randomized, double-blinded, multi-center trial, some subjects with mild TED would be given 100 micrograms of sodium selenite twice a day; others would receive a placebo. Signs, symptoms, and quality of life would be measured at regular intervals throughout the 6 month period of drug administration, and for 6 months thereafter.

Interventions

DRUGSodium selenate

A 100 microgram pill will be orally administered twice a day for 6 months.

DIETARY_SUPPLEMENTSugar pill

The placebo pill will be constructed to look exactly like the selenium pill, but will have no active ingredients. This will be orally administered for 6 months.

Sponsors

International Thyroid Eye Disease Society
CollaboratorUNKNOWN
Columbia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 or older * Able to provide informed consent * Able to swallow pills * Mild thyroid eye disease requiring no past treatment other than ophthalmic drops or ointment * Euthyroid: at least 2 months if on medication irregardless of thyroidectomy status; at least 6 months after radioiodine therapy; if euthyroid for the year prior to enrollment, needs normal thyroid-stimulating hormone (TSH) within last 3 months; if uncontrolled for the year prior to enrollment, needs normal TSH and free T4 within last 3 months; if TSH low, needs normal T3 and free T4 * If you are currently taking any selenium supplementation, you will be asked to discontinue its usage, wash out, for 1 month before you are enrolled.

Exclusion criteria

* Moderate or severe thyroid eye disease (based upon International Thyroid Eye Disease Society VISA form), including: grade 2 chemosis or lid edema; corneal exposure with threat of or resulting in perforation; optic neuropathy; grade 3 restriction of any extraocular muscle * Double vision (diplopia) in primary or reading positions * Duration of thyroid eye disease greater than 12 months (as per patient history) * Drug or alcohol abuse * Severe systemic illness (defined by treating physician) * Pregnant or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Change in Thyroid Eye DiseaseSix months
Difference in Quality of Life scoreSix monthsUsing GO-QOL score

Secondary

MeasureTime frameDescription
Difference in Quality of Life scoreSix monthsTED-PRO
Difference in development of optic neuropathyTwelve months
Difference in Inflammatory IndexSix monthsImprovement
Difference in degrees of restrictionSix monthsImprovement
Difference in exophthalmos scoresSix monthsImprovement
Difference in eyelid apertureSix monthsImprovement
Difference in diplopia scoreSix monthsImprovement
Difference in Clinical Activity ScoreSix months

Other

MeasureTime frame
Fasting glucose levelSix months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026