TESS Shoulder Arthroplasty Data Collection

NCT00751673 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2019-10-08

No results posted yet for this study

Summary

This observational study intends to collect efficacy and safety data on TESS shoulder system

Conditions

Sponsors & Collaborators

  • Biomet France SARL

    collaborator INDUSTRY
  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Laurent BEGUIN, MD · Clinique Mutualiste (Saint Etienne)

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31
Primary Completion
2019-10-31
Completion
2019-10-31

Countries

  • Belgium
  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT00751673 on ClinicalTrials.gov