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Shoulder Instability Trial Comparing Arthroscopic Stabilization Benefits Compared with Latarjet Procedure Evaluation - STABLE Definitive Trial

Shoulder Dislocation | Sport Injuries | Anterior Dislocation

The primary objective of the study is to evaluate the functional shoulder recovery of patients with recurrent shoulder dislocations at 24 months when treated with either arthroscopic capsuloligamentous repair (Bankart Procedure +/- Remplissage) or coracoid transfer (Latarjet procedure).

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 to 50

Participation Criteria

Inclusion Criteria:

1. Adults ages 18-50 years;
2. Diagnosis of post-traumatic recurrent anterior dislocation. This will require a minimum of 2 episodes of documented dislocations either by radiographic evidence or documented reduction of anterior shoulder dislocation as well as physical examination eliciting unwanted glenohumeral translation with reproduction of symptoms;
3. Subcritical glenoid bone loss as defined on CT by standardized and reproducible best-fit circle technique (\>10% but \<20%);
4. Provision of informed consent.

Exclusion Criteria:

1. Patients with concomitant injuries of the index shoulder (cuff tear, greater tuberosity fracture);
2. Previous shoulder surgery;
3. Patients that will likely have problems, in the judgment of the investigators, with maintaining follow-up;
4. Epilepsy/seizure disorder;
5. Patients who are currently incarcerated;
6. Diagnosis of multidirectional instability;
7. Cases involving litigation or workplace insurance claims (e.g. WSIB);
8. Confirmed connective tissue disorder (Ehlers-Danlos, Marfans) or Beighton hypermobility score \> 6.
9. Pregnancy.

Study Location

St. Joseph's Healthcare Hamilton
St. Joseph's Healthcare Hamilton
Hamilton, Ontario
Canada

Contact Study Team

Backup Contact

Moin Khan, MD, MSc,FRCSC

Primary Contact

Miriam Garrido Clua, MSc

[email protected]
Study Sponsored By
McMaster University
Participants Required
More Information
Study ID: NCT05705479