Thyroid Eye Disease
Conditions
Keywords
Antioxidant, Graves' ophthalmopathy, Thyroid eye disease, Severity score, Activity score, Quality of life
Brief summary
This randomized clinical trial is designed to evaluate the effect of selected antioxidant vitamins and minerals supplement named as ASTED: 1. β- Carotene (30 mg) 2. Vit C (100 mg) 3. Vit E (Alpha-Tocopherol Acetate): 60-200 IU 4. Calcium phosphate dihydrate (40 mg) 5. Zinc oxide (4 mg, elemental) 6. Copper gluconate (3.5 mg) 7. Sodium selenite 23 mg= Selenium 100 µg 8. Nicotinamide (a form of vit.B3) (10 mg) in patients with mild Thyroid eye disease according to EUGOGO classification. To be given twice a day.
Detailed description
1. To determine total eye score (NOSPECS severity score) before and after treatment in each of the three arms of the study and make a before - after as well as an inter-arm comparison. 2. To determine Score of thyroid eye disease Quality of life questionnaire (TED-QOL) before and after treatment in each of the three arms of the study and make a before - after as well as an inter-arm comparison. 3. To determine clinical activity score (CAS Score) before and after treatment in each of the three arms of the study and make a before - after as well as an inter-arm comparison. 4. To determine Serum thyroid auto-antibodies (Anti thyroid peroxidase (TPO), Anti-thyrogluboline) and Thyroid function test (Free T4, T3, and TSH) level before and after treatment in each of the three arms of the study and make a before - after as well as an inter-arm comparison. 5. To determine the rate of side effects in each arm and make a comparison.
Interventions
DRUGASTED
A tablet of ASTED will be taken twice a day
DIETARY_SUPPLEMENTSelenium
A tablet of 100 microgram of Selenium (same shape and color) will be taken twice a day
OTHERPlacebo
A tablet of Placebo (same shape and color) will be taken twice a day
Sponsors
Iran University of Medical Sciences
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
1. Mild TED of less than 18 months duration (as recorded by the patient). 2. No active state (Clinical activity score of less than 3). 3. No previous specific therapy for TED, except for local measures (artificial tear, head elevation, low salt diet). 4. Euthyroidism as a result of remission after a course of antithyroid drug (ATD) therapy, or euthyroidism for at least 2 months since commencing ATD or after thyroidectomy, or euthyroidism for at least 6 months after radioiodine therapy. Hypothyroid patients after thyroidectomy or radioiodine were replaced with levothyroxine. Euthyroidism was defined as normal serum free thyroxine, total or free triiodothyronine concentrations, and thyrotropin (TSH) levels below 4 mU/Liter Patients were kept euthyroid for the whole duration of the study. 5. Age 18-70 years.
Exclusion criteria
1. TED severity of more than mild TED. 2. Pregnancy 3. Drug and/or alcohol abuse 4. Severe concomitant illness 5. Inability to comply with the study protocol 6. No informed consent 7. Use of selenium- or vitamin/minerals-containing preparations in the last 3 months. 8. Developing more severe TED in the course of the trial so that requires steroid treatment.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of total eye score (NOSPECS severity score) | 0, 3, 6 months | Change of eye score during the study period |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change of score of thyroid eye disease Quality of life questionnaire (TED-QOL) | 0, 3, 6 months | Change of score of thyroid eye disease Quality of life during study period |
Countries
Iran
Outcome results
None listed