Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
ID04449146

Scapular Positioning in Standing Position Using Sonography

Led by University Hospital, Brest · Updated on 2025-02-12

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the position of the scapula bone in the shoulder while standing and comparing it to its position lying down, using a three-dimensional approach. This study focuses on patients preparing for reverse shoulder arthroplasty surgery and uses a non-radiant, portable system that combines ultrasound with a camera integrated into a tablet to locate the scapula precisely. The study involves a localizer ultrasound performed on patients with their shoulders uncovered to identify key bony landmarks such as the lower angle, coracoid, scapular spine, and acromioclavicular joints. This ultrasound probe is connected to a tablet, which helps to map these points in three dimensions while the patient is standing. The ultrasound is done during a surgical consultation or the day before surgery, taking about half a day. Participants will undergo ultrasound assessment to measure scapular location in three dimensions while standing. Researchers will evaluate the accuracy of the device using a validation bench on the same day. This study is conducted at a single center and involves patients already undergoing pre-operative care for shoulder arthroplasty. The total involvement is brief, focusing on this imaging procedure alongside routine care.

CONDITIONS

Brief Title

Scapular Positioning in Standing Position Using Sonography

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 99 years
  • Agree to participate in the study after receiving oral and written information
  • Patients scheduled for reverse shoulder arthroplasty on a native shoulder joint
Not Eligible

You will not qualify if you...

  • Patients under the age of 18
  • Patients refusing to participate in the study
  • Patients unable to provide informed consent
  • Patients under legal protection such as guardianship, curatorship, or deprived of liberty
  • Patients without health insurance coverage or affiliation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit during surgical consultation or the day before surgery (in-person)

Diagnostic Evaluation

Duration - Half a day

Participants undergo a localizer ultrasound of the shoulder in standing position to locate bony landmarks for 3-dimensional scapular positioning.

1 visit during surgical consultation or admission day before surgery (in-person)

Trial Site Locations

Total: 1 location

1

Brest, University Hospital

Brest, France, 29609

Actively Recruiting

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Research Team

H

Hoel LETISSIER, Dr

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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