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Anatomical Shoulder Domelock System Study

NCT03312465 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 73

Last updated 2026-03-25

No results posted yet for this study

Summary

The objectives of this study are to confirm safety and performance of the Anatomical Shoulder Domelock System when used in hemi or total shoulder arthroplasty by analysis of standard scoring systems, radiographs and adverse event records.

Conditions

  • Avascular Necrosis
  • Revision Surgery
  • Conditions Consequent to Earlier Operations
  • Arthritis, Rheumatoid
  • Arthritis, Degenerative
  • Arthritis;Traumatic

Interventions

DEVICE

AS Domelock System

Hemi or Total Shoulder Arthroplasty

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Emilie Rohmer · Zimmer Biomet Clinical Operations

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-28
Primary Completion
2032-12-09
Completion
2032-12-09

Countries

  • Belgium
  • Germany
  • Switzerland
  • United Kingdom

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 NCT03312465 on ClinicalTrials.gov