OSIRIS Registry
OSIRIS is a prospective clinical registry with the purpose of studying the outcomes of shoulder instability in children and adolescents
Outcomes of Shoulder Instability Research In the Skeletally immature (OSIRIS) – a Clinical Registry
OSIRIS is a prospective clinical registry with the purpose of studying the outcomes of shoulder instability in children and adolescents at the Royal Children’s Hospital, Melbourne, Australia. The registry will collect data pertinent to the diagnosis, treatment and follow-up of shoulder instability in children and adolescents.
The main aims of the OSIRIS registry are to:
Understand the natural history of shoulder instability
Review the outcomes of current treatments
Develop evidence-based treatment strategies that optimise clinical outcomes and standardise care
Research Team
The OSIRIS Registry is overseen by a team of orthopaedic surgeons, clinicians and researchers at the forefront of shoulder instability research:
Dr KW
Lead Principal Investigator & Orthopaedic Surgeon
Pr LD
Principal Investigator & Orthopaedic Surgeon
Dr DE
Principal Investigator & Orthopaedic Surgeon
BM
Research Coordinator
DS
Post-Doctoral Research Assistant
RS
Data Manager
Information for Parents
Below are some frequently asked questions about shoulder instability
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Information for Health Professionals
If you are currently treating a patient who developed shoulder instability at 16 years of age or younger, please consider referring them to the OSIRIS Registry
Physiotherapists
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General Practitioners
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Orthopaedic Surgeons
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Data Collection Is Currently Active
The OSIRIS Registry is currently collecting clinical, radiographic and participant reported outcome measures to help improve outcomes for children and adolescents with shoulder instability.
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