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

NCT03711591 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2020-02-20

No results posted yet for this study

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.

Conditions

  • Proximal Humeral Fracture

Interventions

DEVICE

Conventus Cage PH device

The Conventus CAGE™ PH (PH Cage) is a permanent implant comprised of an expandable scaffold, made from nitinol and titanium, which is deployed into the medullary canal and provides a structure to which fractured bone fragments are attached using fragment screws.

Sponsors & Collaborators

  • Conventus Orthopaedics, Inc.

    lead INDUSTRY

Principal Investigators

  • James M Gregory, MD · The University of Texas Health Science Center, Houston

  • Carrie M Hill · Conventus Orthopaedics, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-29
Primary Completion
2020-02-17
Completion
2020-02-17
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03711591 on ClinicalTrials.gov