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Single Center Post Approval Proximal Humerus Fixation With the Conventus Cage PH™ Device

Proximal Humeral Fracture Clinical Trial

Official title:
Proximal Humerus Fixation With the Conventus Cage™ PH Device A Post-Approval Observational Data Collection Study, A Single-Center Study, Memorial Hermann

Clinical Trial Summary

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

Clinical Trial Description

The study is a prospective, non-randomized, post-market approval data collection study that is designed to collect device/procedure and outcome data on patients who have experienced proximal humerus bone fractures and received a PH Cage.

Specifically, the study will provide:

1. Patient outcome and performance data for the implant and implant procedure that that may be used to support scientific publications.

2. Assurance of continued product safety and effectiveness. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03711591
Study type Observational
Source Conventus Orthopaedics, Inc.
Contact
Status Terminated
Phase
Start date November 29, 2018
Completion date February 17, 2020
View Details
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