Thermal Ablation of Benign Thyroid Nodules with Cryoablation
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- evaluation of technical feasibility
研究概览
简要总结
This study will evaluate the clinical response and safety of ultrasound guided percutaneous cryoablation in the treatment of benign thyroid nodules as an alternative to the surgery. Ablation of functioning or non-functioning benign thyroid nodules with cryoablation will be directed to patients with symptomatic benign thyroid lesions (two benign cytological examinations) measuring between 5 and 65 mL of volume and less than 40% of cystic component; patients must present with serum free thyroxine (T4) and thyroid stimulating hormone (TSH) between the normal range values, with no signs of thyroiditis by serum antibodies over 100% of the standard values; calcitonin levels in the normal range values. Cryoablation will be directed to patients in a non-randomized fashion. Clinical, laboratorial and imaging monitoring will be performed in 12 months, including contrast-enhanced ultrasound when indicated, by 1, 3, 6 and 12 months.
详细描述
Palpable nodular thyroid disease is common in up to 6.4% of the population, and it becomes more common when the thyroid is examined by ultrasound. The vast majority of nodules are benign and, over time, do not change considerably in size. The main treatment indications for a euthyroid patient with a benign thyroid nodule that is not hyperfunctioning are compression of the trachea or esophagus, growth of the nodule, and recurrence of a cystic nodule after aspiration. Other indications for treatment are neck discomfort, cosmetic concern, and patient anxiety about the lump. The main therapeutic options are surgery (unilateral lobectomy) and treatment with thyroxine. Thermal ablative therapy has become a treatment option for solid thyroid lesions, with extensive reports in the medical literature on safety and efficacy with laser and radiofrequency devices, including long-term follow-up studies (10 years). There is no record in the medical literature of the use of cryoablation devices for the ablation of benign thyroid nodules, although they are used for the treatment of tumor lesions in different sites (hepatic, renal, pulmonary, bone and cervical lymph nodes).The objective of this research is to evaluate, in a pilot study, the safety and efficacy of cryoablation in the treatment of benign thyroid nodules.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •18 years of age or older
- •Patients with solitary or dominant functioning or non-functioning thyroid nodules with two consecutive fine needle aspiration biopsy (FNAb)-proven benign in the last 12 months
- •Thyroid nodules should be solid or almost solid (less than 40% of liquid component) with volume between 5 and 65 cc;
- •Patients considered high surgical risk candidates or patients are eligible to surgery who are informed about the ablation therapy and prefers it instead surgery;
- •Calcitonin, thyroglobulin or TSH serum levels in the normal range values
排除标准
- •Age under 18 years
- •Extensive goiter
- •Predominantly cystic nodule with small solid remnant (less than 10%)
- •Nodule volume > 65 cc
- •TSH levels above the normal range
- •Uncorrectable coagulopathy / impossibility to interrupt anticoagulants;
- •Malignant or suspected malignant cytologic specimens;
- •Pregnancy or breast-feeding;
- •Anaplastic or poor-differentiated thyroid carcinoma;
- •Partial thyroidectomy
- •Asymptomatic patients
结局指标
主要结局
evaluation of technical feasibility
时间窗: immediately after ablation
Defined as the ability to puncture the nodule and perform the ablation as preoperatively planned.
2) Incidence of adverse events secondary to the treatment (safety and tolerability) of thermal ablation of benign thyroid nodules
时间窗: up to 4 weeks after ablation
Evaluation of minor and major complication rates, immediately after and 1 month after ablation \[designed as a safety measure: yes\]. The safety endpoint for this study is to evaluate the incidence and severity of the procedure or device-related adverse events, as reported by the CTCAE V5.2017.
次要结局
- Evaluation of technical success(ultrasound examinations 1, 3, 6 and 12 months after ablation)