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Prospective Strength Measurement Involving Muscles Altered In Arthroscopic Latarjet

E

Etzel Clinic

Status

Unknown

Conditions

Shoulder Instability

Treatments

Other: Strength testing before and after arthroscopic Latarjet

Study type

Observational

Funder types

Other

Identifiers

NCT03331510
Prospective Strength Latarjet

Details and patient eligibility

About

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.

Full description

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.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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