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Humeral Head Implants: Radiological and Clinical Evaluation

NCT02754024 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2020-07-14

No results posted yet for this study

Summary

In the past years several shoulder reconstruction systems with different types of prostheses and fixation methods have been developed to improve shoulder arthroplasty, trying to cover a wide range of pathologies and revision situations. The aim of the present study is to report radiological and clinical outcome with a stemless shoulder implant with hollow screw fixation.

Conditions

  • Idiopathic Osteoarthritis
  • Posttraumatic Osteoarthritis
  • Humeral Head Necrosis
  • Instability Arthritis

Interventions

PROCEDURE

Total shoulder arthroplasty (TSA)

stemless humeral head implant: Eclipse™ (Arthrex Inc., Naples, FL, USA)

PROCEDURE

Hemi shoulder arthroplasty (HSA)

stemless humeral head implant: Eclipse™ (Arthrex Inc., Naples, FL, USA)

DEVICE

Eclipse™ (Arthrex Inc., Naples, FL, USA)

stemless humeral head implant

Sponsors & Collaborators

  • Werner Anderl

    lead OTHER

Eligibility

Min Age
40 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-30
Primary Completion
2016-03-31
Completion
2025-09-30

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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 NCT02754024 on ClinicalTrials.gov