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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01247077
Other study ID # DLL-159361
Secondary ID
Status Completed
Phase Phase 2
First received November 23, 2010
Last updated March 30, 2015
Start date November 2008
Est. completion date April 2014

Study information

Verified date March 2015
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority Regional Ethics committé, Stockholm, Sweden':'
Study type Interventional

Clinical Trial Summary

Graves thyrotoxicosis is a common autoimmune disease. Patients suffer at diagnosis from weight loss, increased heart rate and stress intolerance. Some patients have difficulties in regaining quality of life. Diagnosis is found through elevated thyroid hormones thyroxin, suppressed TSH (thyroid stimulating hormone) from the pituitary and elevated stimulatory antibodies, TRAb (thyrotropin receptor antibody) to the thyroid. Selenium is sparse in western Europe. This compound has important function in thyroid hormone metabolism and on the immune system. It is not known whether addition of selenium affects the well being of patients with Graves´thyrotoxicosis. The subject of this study is to investigate this


Description:

In the County of Södermanland we include 44 patients with Graves´thyrotoxicosis. They are treated with methimazole and thyroxin, and randomised to selenium or placebo. Neuropsychological investigation is performed, before medical treatment is commenced and repeated after 9 month. Serum concentration of thyroid hormon levels, autoantibodies and selenium are followed.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date April 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- New diagnose of autoimmune thyrotoxicosis

- biochemically proven with increased thyroxin

- low TSH and elevated TRAb/or positive scintigraphy.

- Age 18 - 55. Willing to participate -

Exclusion Criteria:

- No previous head trauma,

- No difficulties with swedish language,

- No medication which could affective neuropsychological testing,

- No planned or ongoing pregnancies.

- Normal intellectual capacity.

- No severe ophthalmopathy, or other severe disease

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
selenium
200 ug selenium once daily
placebo


Locations

Country Name City State
Sweden Emil Mikulski Eskilstuna
Sweden Jan Calissendorff, Medical clinic, Eskilstuna, Sweden Eskilstuna Södermanland

Sponsors (1)

Lead Sponsor Collaborator
Karolinska Institutet

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effect on neuropsychological well-being Inclusion going on until the end of 2011 No
Secondary Potential effect on autoantibodies Inclusion for the rest of 2011 No