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Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interpositional Implant

NCT02424760 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 67

Last updated 2019-04-16

No results posted yet for this study

Summary

The INSPYRE implant is a new range of shoulder hemi-arthroplasty device. It consists of a Pyrocarbon spherical interpositional implant and is indicated in primary surgery to relieve severe pain or significant disability caused by degenerative pathologies. The rotator cuff must be functional.

The aim of this study is to prospectively collect data from consecutive series to implement a Post Marketing Surveillance plan.

Conditions

  • Localized, Primary Osteoarthritis
  • Post-traumatic Arthrosis of Other Joints, Shoulder Region
  • Avascular Necrosis of the Head of Humerus

Interventions

DEVICE

Shoulder hemi-arthroplasty

Sponsors & Collaborators

  • Stryker Trauma and Extremities

    lead INDUSTRY

Principal Investigators

  • Gilles WALCH, MD · Centre Orthopédique Santy, Lyon, FR

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2021-03-31
Completion
2021-03-31

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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 NCT02424760 on ClinicalTrials.gov