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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04953598
Other study ID # M2018106
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 29, 2018
Est. completion date February 5, 2020

Study information

Verified date June 2021
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study, ultrasound diagnosis was performed for patients with hip joint anterior superior labrum tear, and the final surgical observation was used as the gold standard to evaluate the diagnostic efficacy of ultrasonic measurement of the hip joint anterior superior labrum area in the diagnosis of labrum tear.


Description:

In this study, ultrasound diagnosis was performed for patients with a torn anterior superior labrum of the hip joint, and the final surgical observation was the gold standard. The control group selected patients with non-hip joint reasons to come to the ultrasound department of our hospital for diagnosis at the same time. Both the case group and the control group were included in the study at a rate of 1.1 times. This study plans to include 149 cases in the case group and 297 cases in the control group. This study was used to evaluate the diagnostic efficacy of ultrasonic measurement of the area of the anterior superior labrum of the hip in the diagnosis of labrum tears.


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date February 5, 2020
Est. primary completion date December 14, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 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 1. Age is greater than or equal to 18 years old 2. Patients who come to the ultrasound department of our hospital for treatment of non-hip joints at the same time 3. The patient can understand and sign the informed consent form Exclusion Criteria: Case group exclusion criteria 1. Mental conditions are not allowed 2. 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

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Ultrasonography
Patient undergoes diagnostic ultrasound examination

Locations

Country Name City State
China Department of Ultrasound Diagnosis, Peking University Third Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking University Third Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ultrasound diagnosis result image Ultrasound diagnosis as hip joint anterior superior labrum tear ultrasound diagnosis were preformed with hip arthroscopy at the same 1 day visiting time point
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