Graves Disease Clinical Trial
Official title:
Guiding Methimazole Therapy in Graves' Disease - a Randomised Controlled Trial Comparing a Computer-aided Treatment (Digital Thyroid, DigiThy) Versus Usual Care
The goal of this clinical trial is to compare two methods of guiding methimazole therapy in patients with Graves' disease: methimazole dose adjustments based on a new semi-automated computer-guided treatment (based on a mathematical model) or based on the treating physician's decision (i.e. usual care). The main question it aims to answer is whether semi-automated computer-guided treatment is not inferior to usual care in terms of safety, the time it takes to achieve euthyroidism and the methimazole dose required.
Status | Not yet recruiting |
Enrollment | 52 |
Est. completion date | October 1, 2026 |
Est. primary completion date | October 1, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Active Graves' hyperthyroidism [Thyroid-stimulating hormone <0.1 mU/L, elevated free thyroxine levels (fT4) above the upper limit of normal and positive Thyrotropin receptor antibody (TRAb) according to local laboratory results], measured within the last month prior to the inclusion date - Patients not yet receiving antithyroid treatment, or having received antithyroid treatment continuously for less than 4 weeks, or relapse or recurrence of Graves' hyperthyroidism defined as patients previously having received and discontinued treatment with antithyroid drugs for at least 4 weeks) - Age 18 years or older - Provision of written informed consent Exclusion Criteria: - Previous treatment with radioactive iodine - Ongoing antithyroid treatment for more than one month - Pregnancy - Treatment with propylthiouracil |
Country | Name | City | State |
---|---|---|---|
Austria | Medical University of Graz | Graz |
Lead Sponsor | Collaborator |
---|---|
Medical University of Graz | Graz University of Technology |
Austria,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The primary aim is to compare semi-automated computer-guided treatment with usual care in terms of their performance indices | The performance index is the deviation from the desired free thyroxine (fT4) value | 18 months | |
Secondary | Comparison in terms of cumulative methimazole dosing | Comparison in terms of cumulative methimazole dosing | 18 months | |
Secondary | Comparison based on free thyroxine (fT4) target range | Comparison based on free thyroxine (fT4) target range | 18 months |
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