Standard of care treatment
DeviceSubject has undergone joint space repair using one of the study devices and meets eligibility criteria
NCT Number: NCT06320925
Retrospective, multi-center, chart review (only to include data that is part of the surgeons' standard practice)
Interested in participating?
Request Info18 year and older
All sexes
Observational
Musculoskeletal-Orthopedic Research and Education Foundation, Phoenix, Arizona, United States
The purpose of this study is to leverage standard of care data to provide further characterization of clinical outcomes following shoulder, hip and knee joint surgeries.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subject has undergone joint space repair using one of the study devices and meets eligibility criteria
Time frame: 6 months
Change from baseline
Time frame: 6 months
Change from baseline
Time frame: 6 months
Change from baseline
Contact information is provided by the study sponsor or research team.
Colleen Roden, MS
CONTACT
Hayley Taylor, MS
CONTACT
Stryker Endoscopy
Industry
A Retrospective, Multi-Center, Post-Market Clinical Follow-Up Study of Stryker Class IIb Implants
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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