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GLOBAL ICON Stemless Shoulder System Post Market Clinical Follow Up Study

NCT03168672 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 171

Last updated 2025-08-05

Study results available
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Summary

This is a Post Market Clinical Follow Up (PMCF) study to monitor the safety and performance of the GLOBAL ICON stemless humeral component. The data gathered will be used to support post market surveillance of the device, and may potentially be used for additional market access purposes.

Conditions

Interventions

DEVICE

Global ICON

The study device is the GLOBAL ICON stemless humeral component, consisting of the Anchor Plate and Humeral Head.

Sponsors & Collaborators

  • DePuy Orthopaedics

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-18
Primary Completion
2021-12-13
Completion
2024-06-18

Countries

  • Canada
  • Germany
  • Netherlands
  • United Kingdom

Study Locations

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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 NCT03168672 on ClinicalTrials.gov