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Clinical Trial Summary

The purpose of this study is to collect device and procedure experience in everyday clinical practice. The patients are being asked to participate in this study because they are a surgical candidate for the treatment of a broken shoulder and are considering treatment with the PH Cage device.


Clinical Trial Description

The Conventus CAGE™ PH (PH Cage) System Post-Approval Prospective Study (Study) is a multi-center, prospective, post-approval clinical study designed to collect device and procedure experience in everyday clinical practice.

Specifically, the study will provide:

1. Device safety and patient outcome data.

2. Device usage data.

3. Performance data for the implant procedure.

4. Publications.

5. Early economic benefit data.

Patient Assessments Demographic and general health data will be collected on all patients at the baseline appointment to ensure subjects meet inclusion/exclusion criteria. In addition, to these data, x-rays and adverse event reports related to the implanted device, surgical procedure and/or study data collection methods will be collected.

Patients will be seen at baseline, 2-, 6- and 12-week, 1- and 2-year post op.

Patient participation in this study is voluntary. However, post-implant patient follow-up adds to the medical community's understanding of proximal humerus fracture patient outcomes, as well as the safety and performance of the PH Cage. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03489408
Study type Observational [Patient Registry]
Source Conventus Orthopaedics, Inc.
Contact
Status Terminated
Phase
Start date February 1, 2018
Completion date February 17, 2020

See also
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Completed NCT02425267 - Effectiveness of a Home Telerehabilitation Program for People With Proximal Humerus Fracture N/A
Completed NCT01246167 - Treatment of Proximal Humeral Fractures N/A
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Completed NCT02608801 - Prediction and Secondary Prevention of Fractures