S-ITEDS: Selenium in Mild Thyroid Eye Disease in North America

Sponsor
Columbia University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02112643
Collaborator
International Thyroid Eye Disease Society (Other)
0
2
13.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Sodium selenate
  • Dietary Supplement: Sugar pill
Phase 3

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Selenium - ITEDS: A North American Study
Anticipated Study Start Date :
Oct 1, 2015
Actual Primary Completion Date :
Nov 16, 2016
Actual Study Completion Date :
Nov 16, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Selenium

100 micrograms of sodium selenate will be taken orally twice daily (total 200 micrograms daily) for 6 months.

Drug: Sodium selenate
A 100 microgram pill will be orally administered twice a day for 6 months.
Other Names:
  • Selenium
  • Placebo Comparator: Sugar pill

    A placebo pill will be taken orally twice daily for 6 months.

    Dietary Supplement: Sugar 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.
    Other Names:
  • Placebo
  • Outcome Measures

    Primary Outcome Measures

    1. Difference in Quality of Life score [Six months]

      Using GO-QOL score

    2. Difference in Quality of Life score [Twelve months]

      GO-QOL score

    3. Change in Thyroid Eye Disease [Six months]

    4. Change in Thyroid Eye Disease [Twelve months]

    Secondary Outcome Measures

    1. Difference in Clinical Activity Score [Six months]

    2. Difference in Clinical Activity Score [Twelve months]

    3. Difference in Quality of Life score [Six months]

      TED-PRO

    4. Difference in Quality of Life score [Twelve months]

      TED-PRO

    5. Difference in Quality of Life score [Six months]

      TED-QOL

    6. Difference in Quality of Life score [Twelve months]

      TED-QOL

    7. Difference in development of optic neuropathy [Twelve months]

    8. Difference in Inflammatory Index [Six months]

      Improvement

    9. Difference in Inflammatory Index [Twelve months]

      Improvement

    10. Difference in Inflammatory Index [Six months]

      Deterioration

    11. Difference in Inflammatory Index [Twelve months]

      Deterioration

    12. Difference in diplopia score [Six months]

      Improvement

    13. Difference in diplopia score [Twelve months]

      Improvement

    14. Difference in diplopia score [Six months]

      Deterioration

    15. Difference in diplopia score [Twelve months]

      Deterioration

    16. Difference in degrees of restriction [Six months]

      Improvement

    17. Difference in degrees of restriction [Twelve months]

      Improvement

    18. Difference in degrees of restriction [Six months]

      Deterioration

    19. Difference in degrees of restriction [Twelve months]

      Deterioration

    20. Difference in exophthalmos scores [Six months]

      Improvement

    21. Difference in exophthalmos scores [Twelve months]

      Improvement

    22. Difference in exophthalmos scores [Six months]

      Deterioration

    23. Difference in exophthalmos scores [Twelve months]

      Deterioration

    24. Difference in eyelid aperture [Six months]

      Improvement

    25. Difference in eyelid aperture [Twelve months]

      Improvement

    26. Difference in eyelid aperture [Six months]

      Deterioration

    27. Difference in eyelid aperture [Twelve months]

      Deterioration

    Other Outcome Measures

    1. Fasting glucose level [Six months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts 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

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Columbia University
    • International Thyroid Eye Disease Society

    Investigators

    • Principal Investigator: Micahel Kazim, MD, International Thyroid Eye Disease Society

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Columbia University
    ClinicalTrials.gov Identifier:
    NCT02112643
    Other Study ID Numbers:
    • AAAL9502
    First Posted:
    Apr 14, 2014
    Last Update Posted:
    Aug 18, 2021
    Last Verified:
    Aug 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Columbia University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 18, 2021