High Intensity Focused Ultrasound Clinical Trial
Official title:
A Randomized, Open-label, Parallel-group Study to Determine the Efficacy of Sequential High-intensity Focused Ultrasound (HIFU) Ablation Versus Fixed-dose Radioiodine-131 Therapy in Moderate-sized Non-toxic Multinodular Goiter
NCT number | NCT04009863 |
Other study ID # | UW 19-016 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 1, 2020 |
Est. completion date | April 30, 2022 |
Verified date | May 2022 |
Source | The University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
After obtaining informed consent, eligible subjects will be assigned randomly into either High intensity focused ultrasound group (HIFU) or Radioactive iodine (131I) therapy group (RAIT). After treatment, they will be followed up for 4 visits (1-month, 3-month, 6- month, 12-month of post treatment). At each visit, they will have physical examination, regular blood test and questionnaire to evaluate their quality of life. The collected data will be used to compare the effectiveness between HIFU and RAIT for non-toxic multi-nodular goiter (NMNG). The primary purepose is to find out the best non-invasive way in treating NMNG. For HIFU, you may experience: 1. Mild bruising and redness at the site of treatment 2. Edema of the skin tissue 3. Pain/discomfort during the procedure 4. Skin burns but rare (<1%) 5. Vocal cord paresis on the side of the treated lobe but rare (<1%) 6. Unintentional damage to the surrounding tissue (outside the planned treatment area). For RAIT, you may experience neck tenderness or sore throat in the following few days as developing moderate inflammation in the thyroid and producing discomfort in the neck or throat area. Your symptoms may turn worse for first few week, but will improve over weeks.
Status | Completed |
Enrollment | 156 |
Est. completion date | April 30, 2022 |
Est. primary completion date | February 20, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Have a moderate-sized NMNG. The dimension of the largest nodule cannot exceed 50mm in diameter. Also on USG volumetry, the total combined volume of the three largest nodules (i.e. the largest nodule volume + second largest nodule volume + third largest nodule volume) or in short, TNV cannot exceed 80 mL or cm^3. - The NMNG has to benign. Each nodule within the goiter will be carefully evaluated on USG by an experienced clinician to look for suspicious features for malignancy. Suspicious-looking nodules will be biopsied by USG-guided FNAC. Only nodules with Bethesda II on FNAC will be considered benign. - Aged between 18 and 70 years old at the time of informed consent. - Have genuine cosmetic and/or pressure symptoms. - Have to have normal serum free T4 (FT4) and thyroid-stimulating hormone (TSH) levels. Exclusion Criteria: - Have a non-toxic diffuse goiter or a NMNG with the largest nodule < 20mm in diameter. - Prefer or have a clear indication for thyroidectomy (such as rapidly growing, compressive goiter or suspected or documented thyroid malignancy). - Have a pre-existing vocal cord palsy. - Unable to tolerate even slight neck extension during HIFU ablation. - Pregnant, lactating women or women wishing to become pregnant within 6 months. - Previous thyroid surgery or neck irradiation. - Family history of non-medullary thyroid carcinoma. - Have any medical conditions that would make them too ill to undergo treatment. |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Queen Mary Hospital | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
The University of Hong Kong |
Hong Kong,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The absolute change in Thyroid nodule volume (TNV) after sequential HIFU treatment and a fixed-dose (370MBq) RAIT after 12 months. | To compare the absolute change in Thyroid nodule volume (in cm^3) after sequential HIFU treatment and a fixed-dose (370MBq) RAIT after 12 months. | 12 months | |
Secondary | Change in total thyroid volume (TTV) (in cm^3) | To compare the absolute change in TTV between HIFU and RAIT groups | 12 months | |
Secondary | Change in the largest/dominant nodule dimensions | To compare the change in the largest/dominant nodule dimensions (in cm) between HIFU and RAIT groups | 12 months | |
Secondary | Incidence of treatment-related morbidities after HIFU/RAIT | To compare incidence of treatment-related morbidities and hypothyroidism between HIFU and RAIT groups | 12 months | |
Secondary | Change in World Health Organization goiter grade | To compare WHO goiter grade over time between HIFU and RAIT groups | 12 months | |
Secondary | Change in symptom improvement score | To compare symptom improvement score (0-10) over time between HIFU and RAIT groups | 12 months | |
Secondary | Change in pressure symptom score | To assess the changes in pressure symptom score (by Visual Analogue Scale, VAS, scoring from 0-10, 0 is for no pressure and 10 is for the maximum pressure feeling as subjects' view) over time between the HIFU and RAIT groups. | 12 months | |
Secondary | Change in quality of life | To assess the changes in quality of life (QOL) using by "12-Item Short Form Survey (SF-12) (VERSION 2.0)" between the two treatment groups. SF-12 is scoring 70 in total, the higher score represent higher quality of life. | 12 months | |
Secondary | Change in patient satisfaction | To assess the changes in patient satisfaction (by Visual Analogue Scale, VAS, scoring from 0-10, 10 is for the maximum score representing well satisfaction) between the two treatment groups | 12 months | |
Secondary | Compare the costs (in dollars) | To compare the direct and indirect costs between HIFU and RAIT (in dollars) | 12 months |
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