Research on Optimization of Rotator Cuff Injury Diagnosis Plan

July 21, 2021 updated by: Peking University Third Hospital

Rotator cuff injury is a common cause of shoulder pain and dysfunction. Finding out patients with suspected rotator cuff injuries through physical examination of the shoulder joints, MRI further assists in the diagnosis, and final surgical diagnosis and treatment are the current standardized procedures.

How to apply multiple physical examination programs to make judgments sensitively, efficiently and accurately is a clinical problem that needs to be solved urgently.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Rotator cuff injury is a common cause of shoulder pain and dysfunction. The common symptoms of rotator cuff injury include shoulder pain, weakness, and limited mobility. Arthroscopic exploration is the gold standard for the diagnosis of rotator cuff injury, but it is an invasive examination that is difficult to carry out routinely; MRI is sensitive in diagnosing rotator cuff tears Both sex and specificity are high, but due to the popularity, cost and waiting time, it is difficult to be used as a routine screening method.

Therefore, finding patients with suspected rotator cuff injuries through physical examination of the shoulder joints, MRI further assisting in the diagnosis, and final surgical diagnosis and treatment are the current standardized procedures.

However, although there are many physical examination methods for the shoulder joint, the accuracy of each method is different, and each has its own sensitivity and specificity. How to apply multiple examination programs in combination to make it sensitive, efficient and accurate Judgment is a problem that needs to be solved clinically.

This study is expected to adopt prospective research methods to collect and collect patient medical records, preoperative physical examination results, imaging data, and findings during intraoperative exploration, to understand the impact of various shoulder joint physical examination methods and imaging data on rotator cuff injuries

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 55 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with shoulder pain who were treated at peking university's Third Hospital outpatient clinic for a continuous period of time

Description

Inclusion Criteria:

  • Patients who are prepared to undergo arthroscopic surgery for shoulder injuries

Exclusion Criteria:

  • Shoulder stiffness, shoulder instability, calcified tendinitis, past surgery, side-to-shoulder disease, hamada osteoarthritis, frozen shoulder, acute joint injury, rheumatoid arthritis, hyperuricemia

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients with shoulder pain who received ER lag sign
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury
Patients with shoulder pain who received External rotation resistence strength test
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury
Patients with shoulder pain who received Patte's test
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury
Patients with shoulder pain who received Errsair test
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury
Patients with shoulder pain who received speed test
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury
Patients with shoulder pain who received Yergason test
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury
Patients with shoulder pain who received backward traction test
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury
Patients with shoulder pain who received Cui's test
By using physical examinations, the incidence of these physical examinations corresponding to shoulder muscls injury

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
the Accuracy of different physical examinations
Time Frame: 1week
After apply these physical examinations, by using Arthroscopic examination find the accuracy of these physical examinations
1week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Guoqing Cui, MD, Peking University Third Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

September 1, 2021

Primary Completion (Anticipated)

September 1, 2022

Study Completion (Anticipated)

June 1, 2023

Study Registration Dates

First Submitted

July 21, 2021

First Submitted That Met QC Criteria

July 21, 2021

First Posted (Actual)

July 22, 2021

Study Record Updates

Last Update Posted (Actual)

July 22, 2021

Last Update Submitted That Met QC Criteria

July 21, 2021

Last Verified

July 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • M2021099

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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