Humeral Head Implants: Radiological and Clinical Evaluation

Werner Anderl

Status: Active, not recruiting

Conditions: Humeral Head Necrosis; Idiopathic Osteoarthritis; Posttraumatic Osteoarthritis; Instability Arthritis

Treatments: Device: Eclipse™ (Arthrex Inc., Naples, FL, USA); Procedure: Total shoulder arthroplasty (TSA); Procedure: Hemi shoulder arthroplasty (HSA)

Study type: Observational

Funder types: Other

Identifiers

NCT02754024

HHI

Details and patient eligibility

About

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.

Enrollment: 100 estimated patients

Sex: All

Ages: 40 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 40 to 85 years at time of surgery
• Patients with primary or secondary osteoarthritis of the shoulder

Exclusion criteria

• Patients with cuff tear arthropathy and axillary nerve lesions

Trial design

100 participants in 2 patient groups

Total shoulder arthroplasty (TSA)

Description:

Replacement of humeral head and glenoid

Treatment:

Procedure: Total shoulder arthroplasty (TSA)

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

Hemi shoulder arthroplasty (HSA)

Description:

Replacement of humeral head only

Treatment:

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

Procedure: Hemi shoulder arthroplasty (HSA)