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Graves' disease (GD) is the most frequent cause of hyperthyroidism in iodine sufficient countries and Graves' orbitopathy (GO) is its most common extrathyroidal manifestation. Restoration and maintenance of euthyroidism are imperative in Graves' disease patients with GO. The main treatment options for Graves' hyperthyroidism are antithyroid drugs, radioactive iodine (RAI), and surgery. Whether one or the other therapy for Graves' hyperthyroidism offers the best protection against GO is not established. The study is aimed at comparing the effects of a conservative approach (antithyroid drugs, ATDs, experimental arm) vs an ablative approach (radioiodine or total thyroidectomy) of thyroid treatment on the overall outcome of GO in patients with GD and moderate-to-severe and active GO treated with intravenous glucocorticoids.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Methimazole | Experimental | Antithyroid drugs (at individualized dosage) for 72 weeks and a cumulative dose of 4.5 g of methylprednisolone divided into 12 weekly infusions |
|
| Thyroid ablation | Active Comparator | Radioiodine therapy or total thyroidectomy (according to ultrasound thyroid volume) and a cumulative dose of 4.5 g of methylprednisolone divided into 12 weekly infusions |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Methimazole | Drug | Methimazole for 72 weeks |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Overall GO outcome | Improvement is defined as change in two of the following outcome measures in at least one eye, without deterioration in any of the same measures in both eyes (compared to baseline):
Patients meeting the improvement criteria will be considered as "responders". All other patients will be considered as "non-responders". | 24 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Overall GO outcome | Improvement is defined as change in two of the following outcome measures in at least one eye, without deterioration in any of the same measures in both eyes (compared to baseline):
Patients meeting the improvement criteria will be considered as "responders". All other patients will be considered as "non-responders". |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Michele Marino | Contact | +39050997346 | michele.marino@med.unipi.it | |
| Giulia Lanzolla | Contact | +39050997346 | giulia.lanzolla8@gmail.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Endocrinology Unit II | Recruiting | Pisa | PI | 56124 | Italy |
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| ID | Term |
|---|---|
| D049970 | Graves Ophthalmopathy |
| ID | Term |
|---|---|
| D015785 | Eye Diseases, Hereditary |
| D005128 | Eye Diseases |
| D006111 | Graves Disease |
| D005094 | Exophthalmos |
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| ID | Term |
|---|---|
| D008713 | Methimazole |
| C000614965 | Iodine-131 |
| D013965 | Thyroidectomy |
| ID | Term |
|---|---|
| D013438 | Sulfhydryl Compounds |
| D013457 | Sulfur Compounds |
| D009930 | Organic Chemicals |
| D007093 | Imidazoles |
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| Radioiodine or thyroidectomy | Procedure | Treatment with radioiodine or with thyroidectomy |
|
|
| 48 weeks |
| Overall GO outcome | Improvement is defined as change in two of the following outcome measures in at least one eye, without deterioration in any of the same measures in both eyes (compared to baseline):
Patients meeting the improvement criteria will be considered as "responders". All other patients will be considered as "non-responders". | 72 weeks |
| Response of individual GO parameters: proptosis, CAS, eyelid width, diplopia, and visual acuity | Improvement is defined as change in each of the following outcome measures in at least one eye, without deterioration in both eyes (compared to baseline):
Patients meeting the improvement criteria will be considered as "responders". All other patients will be considered as "non-responders". | 24, 48 and 72 weeks |
| Quality of life questionnaire | Comparison of a disease specific quality of life questionnaire (GO-QoL) at 24, 48 and 72 weeks. Positive response: an improvement in the questionnaire by at least 6/48 points. The GO-QoL contains 8 questions on visual functioning and 8 questions on appearance. The minimal clinically important difference in scores is ≥ 10 points for invasive therapies, but a change of 6 is already perceived by patients as beneficial and is associated with an important change in daily functioning. The GO-QoL is well validated, widely used, and available in eight languages. The GO-QoL is recommended as an independent outcome measure in randomized clinical trials24. | 24, 48 and 72 weeks |
| D009916 |
| Orbital Diseases |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D006042 | Goiter |
| D013959 | Thyroid Diseases |
| D004700 | Endocrine System Diseases |
| D006980 | Hyperthyroidism |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
| D001393 |
| Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D013507 | Endocrine Surgical Procedures |
| D013514 | Surgical Procedures, Operative |