Prospective Strength Measurement Involving Muscles Altered In Arthroscopic Latarjet

NCT ID: NCT03331510

Last Updated: 2017-12-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-02-28

Study Completion Date

2022-12-31

Brief Summary

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Open and arthroscopic Latarjet procedures are used to treat shoulder instability as primary and salvage procedures. During surgery the coracoid process is detached and repositioned to the anterior glenoid through a subscapularis split and fixed in place, resulting in an enlarged glenoid and therefor articular surface. However, before this is done, the pectorals minor, which inserts at the coracoid process, has to be detached and is left without further treatment. Moreover, the conjoint tendon, the origin of the short head of the biceps and coracobrachialis, is repositioned with the coracoid and therefor distalized and medialized.

No study currently followed up on the strength of the muscles altered. The aim of this study is therefor, to prospectively measure range of motion and strength of the operated shoulder at different time points pre- and postoperatively, comparing it with the healthy shoulder in each individual.

Detailed Description

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Strength, range of motion and stability will be assessed pre-operatively and at 6 weeks, 12 weeks, 6 months, 12 months and 24 months post-operatively. Next to standard radiological follow up, including X-ray, arthrographic computed tomography as well as arthrographic magnetic resonance imaging, specific shoulder scores will be utilised. Strength for general shoulder motion as well as specifically for the subscapularis, the pectorals minor, the coracobrachialis and the biceps will be measured with a shoulder dynamometer. Data will be analysed and published.

Conditions

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Shoulder Instability

Keywords

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Shoulder, Instability, Latarjet, Dislocation, Strength

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Strength testing before and after arthroscopic Latarjet

After patients, based on the ISI-Score, were assigned to treat their shoulder instability with an arthroscopic Latarjet procedure, they are eligible for this study. Strength of different involved muscles, as well as ROM will be measured before and at several time points after surgery.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients who experienced at least one shoulder dislocation.
* Patients who are willing to participate in the study
* Patients who receive arthroscopic Latarjet procedure for treatment of glen-humeral instability
* Patients who are at least 18 years old.
* Patients with an ISI-Score of at least 4 points.

Exclusion Criteria

* Patients older than 50 or younger than 18 years of age.
* Patients with painful unstable (multidirectional) instability
* Patients with congenital defects of the bones involved (humerus, scapula).
* Patients with an ISIS of smaller 4 points.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Etzel Clinic

OTHER

Sponsor Role lead

Responsible Party

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Daniel Smolen, MD

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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Prospective Strength Latarjet

Identifier Type: -

Identifier Source: org_study_id