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临床试验/NCT05982821
NCT05982821已完成不适用

A Multicenter Study of Artificial Intelligence-assisted Contrast-enhanced Ultrasound Diagnosis of Thyroid Nodules

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University1 个研究点 分布在 1 个国家目标入组 1,955 人开始时间: 2023年6月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,955
试验地点
1
主要终点
Diagnostic performance

研究概览

简要总结

The goal of this intervention study is to learn about the diagnostic performance of artificial intelligence to assist the contrast-enhanced ultrasound diagnosis of thyroid nodules. The main questions it aims to answer are:

  1. Can we develop an artificial intelligence model to assist the contrast-enhanced ultrasound diagnosis of thyroid nodules?
  2. Can artificial intelligent reduce the unnecessary biopsy of thyroid nodules?

Participants will be asked to undergo contrast-enhanced ultrasound examination and ultrasound-guided fine-needle aspiration of thyroid nodules. Researchers will calculate the diagnostic performance of the contrast-enhanced ultrasound diagnosis of thyroid nodules with and without artificial intelligent assistance.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

盲法说明

Cytopathologists, histopathologists and statistical analysts were blinded to the intervention.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with thyroid nodules with a solid component ≥5 mm confirmed by conventional ultrasound;
  • Patients who underwent conventional ultrasound, contrast-enhanced ultrasound, and fine-needle aspiration biopsy;
  • Patients with a final benign or malignant pathological results.

排除标准

  • Patients with cytopathology of Bethesda I, III, or IV and without final benign or malignant pathology;
  • Patients with a history of thyroid ablation or surgery;
  • Patients with low-quality ultrasound images.

结局指标

主要结局

Diagnostic performance

时间窗: First week after primary completion date.

Sensitivity, specificity, positive predictive value, negative predictive value, accuracy, area under the curve

The necessity of biopsy

时间窗: First week after primary completion date.

Unnecessary biopsy rate

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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