Clinical Trials

Inclusion Criteria:

- Civilians and military personnel ages 17 to 50

- Traumatic anterior shoulder dislocation

- Associated subcritical bone loss between 10-20% less the glenoid width quantified by
standard of care CT scan

Exclusion Criteria:

- Chronic, non-traumatic multi-directional instability based on clinical exam.

- Concurrent shoulder injury (e.g. rotator cuff tears, motor nerve pathologies,
osteoarthritis of a Samilson-Prieto grade >2).

- Prior instability or rotator cuff procedure on involved shoulder (including
intra-articular soft tissue surgery).

- Humeral sided bone lesion (Hill-Sachs lesion) that is sufficiently large enough to
render the lesion "off-track" even after a bony augmentation procedure would be
performed.

- Neuromuscular and other movement control pathologies including seizures.

- Vascular injury associated with the shoulder trauma.

- Traumatic brain injury or any condition that would preclude the ability to comply with
post-operative guidelines.

- Does not plan to return to pre-injury levels of work, sports or military duty.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 11/9/22. Questions regarding updates should be directed to the study team contact.