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临床试验/NCT04966728
NCT04966728已完成不适用

Ultrasonic Diagnosis of Tear of the Anterior Superior Labrum of the Hip

Peking University Third Hospital1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2018年5月15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
180
试验地点
1
主要终点
Comparison of conventional ultrasound diagnosis of the hip joint and arthroscopic diagnosis results

研究概览

简要总结

The patients were divided into two groups, one group was a suspected hip joint anterior superior labrum tear, and the other group was a non-hip joint disease. The patients received conventional ultrasound diagnosis of the hip joint, contrast-enhanced ultrasound, and high-resolution single hip MRI for surgery Perform diagnostic power test for the gold standard.

详细描述

The patients were divided into two groups, one group was patients with suspected anterior superior labrum tear, and the other group was patients with non-hip joint diseases. Routine ultrasound diagnosis of the hip, contrast-enhanced ultrasound, and high-resolution single hip MRI were performed. For patients undergoing hip arthroscopic surgery after diagnostic occlusive treatment, the results of arthroscopic exploration are used as the diagnostic gold standard. A tear detected during the operation was judged to be positive, and a tear not detected was judged to be negative. For patients who have not undergone hip arthroscopic surgery after the closure treatment, if the MRI of the hip is performed, the MRI result is the gold standard. The diagnosis of tearing was judged as positive, and the undiagnosed tearing was judged as negative. This study was used to compare (1) the diagnostic efficacy of hip joint contrast-enhanced ultrasound and high-resolution single hip MRI in patients with suspected anterior superior labrum tear. (2) Comparison of the diagnostic efficiency of contrast-enhanced hip joint ultrasound and conventional ultrasound in patients with suspected anterior superior labrum tear. (3) In the process of judging the hip joint anterior superior labrum tear by conventional ultrasound and contrast-enhanced ultrasound of the hip joint, the consistency of repeated readings and the comparison of the consistency between readers.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • Case group inclusion criteria (1) Age is greater than or equal to 18 years old (2) Patients with preoperative ultrasound examination for clinically planned hip joint anterior superior labrum tear (3) The patient can understand and sign the informed consent form .
  • Control group inclusion criteria
  • Age is greater than or equal to 18 years old
  • Patients who come to the ultrasound department of our hospital for treatment of non-hip joints at the same time
  • The patient can understand and sign the informed consent form

排除标准

  • Case group exclusion criteria
  • Mental conditions are not allowed
  • Adhesives that are allergic to any known . Control group exclusion criteria (1) Mental conditions are not allowed (2) Adhesives that are allergic to any known (3) Past and current diseases of other hip joint diseases

结局指标

主要结局

Comparison of conventional ultrasound diagnosis of the hip joint and arthroscopic diagnosis results

时间窗: Hip arthroscopy was performed 1 week after ultrasound diagnosis of the hip joint.

Comparison of conventional ultrasound diagnosis of the hip joint and arthroscopic diagnosis results

Comparison of conventional contrast-enhanced ultrasound diagnosis of the hip joint and arthroscopic diagnosis results

时间窗: Hip arthroscopy was performed 1 week after conventional contrast-enhanced ultrasound diagnosis of the hip joint.

Comparison of conventional contrast-enhanced ultrasound diagnosis of the hip joint and arthroscopic diagnosis results

Comparison of high-resolution single MRI diagnosis of the hip joint and arthroscopic diagnosis results

时间窗: Hip arthroscopy was performed 1 week after high-resolution single MRI diagnosis of the hip joint.

Comparison of high-resolution single MRI diagnosis of the hip joint and arthroscopic diagnosis results

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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