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ASHCOM Shoulder System and Its Related Instruments

NCT04258605 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2025-04-03

Study results available
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Summary

The objectives of this study are to confirm safety, performance and clinical benefits of the ASHCOM Shoulder System and its related instruments by analysis of standard scoring systems, radiographs and adverse event records.

Conditions

  • Rotator Cuff Injuries
  • Shoulder Pain
  • Arthropathy; Traumatic
  • Arthroplasty Complications

Interventions

DEVICE

ASHCOM Shoulder System

Reverse Shoulder Arthroplasty

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Marcello Stamilla, MD · Clinica del Mediterraneo

Eligibility

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

Timeline & Regulatory

Start
2019-12-10
Primary Completion
2023-12-18
Completion
2024-08-13

Countries

  • Italy

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 NCT04258605 on ClinicalTrials.gov