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Multicenter Clinical Observation PROMOS®

NCT02280499 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 87

Last updated 2016-03-21

Study results available
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Summary

Overall study design:

This study is a prospective, multicenter, postmarket clinical observation to validate the PROMOS™ Standard Shoulder System as state-of-the-art implant system for total shoulder arthroplasty in terms of radiographic and clinical performance as well as long-term survivorship over 10 years.

Conditions

  • Primary and Secondary Omarthrosis

Interventions

DEVICE

standard PROMOS prosthesis

Sponsors & Collaborators

  • Smith & Nephew Orthopaedics AG

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-11-30
Primary Completion
2015-03-31
Completion
2015-03-31

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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 NCT02280499 on ClinicalTrials.gov