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This study evaluates the efficacy of the HIFU for the treatment of benign thyroid nodules with the FastScan version using assessment of patient experience and adverse event reporting.
Echopulse is specially designed, manufactured and CE marked for treating benign thyroid nodules. HIFU is a completely alternative to surgery which utilizes high-energy ultrasound to deliver a large amount of sound energy to a focal point to rapidly induce tissue heating to 85-90°C.This initiates tissue coagulation followed by tissue necrosis ablating the targeted area.
In a previous european feasibility study performed at 1 site (Bulgaria), 20 benign thyroid nodules were treated. The HIFU treatment was well tolerated and showed efficacy.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Echopulse | Experimental | Echopulse HIFU |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Echopulse | Device | HIFU Under ultrasound guidance |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with adverse events | 1 day post treatment | |
| Number of participants with adverse events | 3 days post treatment | |
| Number of participants with adverse events | 7 days post treatment | |
| Change in volume of the thyroid nodule compared to Baseline at 6 months | 6 months post treatment | |
| Change from Baseline Patient pain intensity score (100mm visual analog scale) at 1 day | 1 day post treatment | |
| Change from Baseline Patient pain intensity score (100mm visual analog scale) at 3 days | 3 days post treatment | |
| Change from Baseline Patient pain intensity score (100mm visual analog scale) at 7 days | 7 days post treatment | |
| Patient satisfaction questionnaire | 6 months post treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Number of patients with Absence of palpable lesion | 3 months post treatment | |
| Number of patients with Absence of palpable lesion | 6 months post treatment | |
| Patient Cosmetic evaluation measured by questionnaire |
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Inclusion Criteria:
Male or female patient 18 years or older.
Patient presenting with at least one thyroid nodule with no signs of malignancy:
Normal TSH (thyroid-stimulating hormone)
Targeted nodule accessible and eligible to HIFU
Absence of abnormal vocal cord mobility at laryngoscopy
Nodule diameter ≥ 10mm measured by ultrasound
Composition of the targeted nodule(s) : predominantly solid
Patient has signed a written informed consent.
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Roussanka Kovatcheva, Prof. | roussanka_kov@yahoo.com | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital of Endocrinology USBALE | Sofia | 1431 | Bulgaria |
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| 6 months post treatment |
| Investigator rated evaluation of the device | Post treatment Day 0 |
| Change from Baseline of gland vascularization at 3 months | 3 months post treatment |
| Change from Baseline of gland vascularization at 6 months | 6 months post treatment |