Arthrex Eclipse™ Shoulder Prosthesis



Status:Active, not recruiting
Conditions:Arthritis, Osteoarthritis (OA)
Therapuetic Areas:Rheumatology
Healthy:No
Age Range:21 - Any
Updated:12/14/2018
Start Date:January 2013
End Date:December 2020

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A Prospective, Randomized, Multicenter Study Comparing the Safety and Effectiveness of Arthrex's Eclipse™ Shoulder Prothesis to the Univers™ II Shoulder Prosthesis in Patients With a Degenerative Joint Disease

A Prospective, Randomized, Multicenter Study comparing the Safety and Effectiveness of
Arthrex's Eclipse™ Shoulder to the Univers™ II Shoulder Prosthesis in patients with a
degenerative joint disease.

The purpose of this study is to demonstrate non-inferiority of the Arthrex Eclipse™ Shoulder
Prosthesis to the Arthrex Univers™ II Shoulder Prosthesis for the treatment of degenerative
joint disease in subjects who are candidates for total shoulder replacement. Non-inferiority
in terms of safety and effectiveness will be measured by a 2 year composite clinical success
(CCS) that requires functional improvement, radiographic success, absence of reoperations and
revision, and lack of serious device-related adverse events.

Inclusion Criteria:

- The subject is > 21 years of age

- The subject has continued symptoms in target shoulder despite at least 3 months of
other treatment modalities(e.g.: anti-inflammatory, physical therapy and steroid
injections)

- The subject has a diagnosis in the target shoulder of one or more of the following:

osteoarthritis, avascular necrosis, post-traumatic arthritis, or rheumatoid arthritis.

- The subject presents with pain and functional impairment in the index shoulder,
measured by an Adjusted Constant Score of ≤50. Note: The Adjusted Constant Score will
be calculated from the raw Constant Score to establish patient eligibility.

- The subject is willing to receive implantation of the Arthrex™ Shoulder Prosthesis or
Univers™ II Shoulder Prosthesis.

- The subject must be physically and mentally willing and able to comply with all study
procedures (including follow-up visits and radiographic assessments) until the
conclusion of the study.

- The subject has been informed of the nature of the study and provided written consent
as approved by the sites local Institutional Review Board or Ethic Review Board.

Exclusion Criteria:

- The subject is likely a candidate for hemi-humeral arthroplasty (i.e.: Avascular
Necrosis of the humeral head without glenoid involvement (Stages 0-3): Rotator Cuff
Deficient Shoulder: Glenoid Bone deficiency/deformity that precludes glenoid
replacement (Walch Type B2 or C) or Fractures of the Proximal Humerus, without Glenoid
involvement.

- The subject has immature bone as defined by the absence of cancellous bone patterning,
a mature, thick cortex, and stress lines within the cancellous bone.

- The subject has obvious defects in bone quality, such as cysts or lesions, in the
humeral head of the target shoulder, as demonstrated by radiographic evaluation.

- The subject has a target shoulder a rotator cuff that is not intact and not
reconstructible.

- The subject has Irreducible 3- and 4- part proximal humeral fractures of the target
shoulder.

- The subject has documented history of foreign-body sensitivity.

- Subject with positive pregnancy test, or lactating, or intends to become pregnant
during treatment period

- The subject has history of Schizophrenia, Bipolar Disorder and/or Major Depressive
Disorder as defined by DSM IV.

- The subject is skeletally immature demonstrated radiographically by incomplete closure
of proximal humeral epiphyses.

- The subject is at high risk for poor healing or confounding outcomes [(i.e.:
clinically significant renal, hepatic, cardiac hematologic disease or endocrine
disease)]

- The subject is on immune-stimulating or immunosuppressive agents

- The subject has co-morbidity that reduces life expectancy < 36 month.

- The subject seeking or receiving workman's compensation for shoulder injury,

- The subject is > 350 lbs.

- The subject engaged in heavy labor (e.g. repetitive lifting in the excess of more than
50 lbs.)

- The subject has had surgery in the affected shoulder in the last 12 months (with the
exception of diagnostic arthroscopy without reconstruction or repair procedures)

- The subject is engaged in active sports participation. (e.g. weight lifting involving
upper extremities or involved in contact sports)

- The subject is taking medications known to potentially interfere with bone/soft tissue
healing (e.g. steroids with the exception of topical and/or inhalers)

- The subject is a prisoners or wards of the state

- The subject has a history of alcohol and/or substance abuse as defined by DSM IV
(Diagnostic and Statistical Manual Diploma in Social Medicine)

- The subject has an active or chronic infection, either systemic or local.

- The subject has pathologic fractures of the affected shoulder

- The subject has acute trauma of the affected shoulder

- The subject has osteoporosis defined as a bone density T score of < or = -2.5. (A
screening Questionnaire for osteoporosis, SCORE (Simple Calculated Osteoporosis Risk
Estimation) and MORES (Male Osteoporosis Risk Estimation Score), will be used to
screen patients who require a DEXA (dual energy x-ray absorptiometry) bone mineral
density measurement.
We found this trial at
16
sites
Sun City, Arizona 85351
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3000 Fairway Drive
Altoona, Pennsylvania 16602
Principal Investigator: Joshua Port, MD
Phone: 814-944-4532
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Altoona, PA
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Amherst, New York 14226
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Amherst, NY
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Chicago, Illinois 60612
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Chicago, IL
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ChillIcothe, Ohio 45601
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ChillIcothe, OH
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Columbia, SC
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Columbus, Ohio 43215
Principal Investigator: Nathan Long, D.O.
Phone: 614-566-8394
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Columbus, OH
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Denver, Colorado 80218
Principal Investigator: Benjamin Sears, MD
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Denver, CO
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Duluth, Minnesota 55805
Principal Investigator: Jeffery Klassen, MD
Phone: 218-786-4126
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Duluth, MN
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East Syracuse, New York 13057
Principal Investigator: Kevin Setter, M.D.
Phone: 315-464-8618
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East Syracuse, NY
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Hyattsville, Maryland 20782
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Hyattsville, MD
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Louisville, Kentucky 40223
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Louisville, KY
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Medford, Oregon 97504
Principal Investigator: Patrick Denard, MD
Phone: 701-430-2097
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Medford, OR
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Philadelphia, Pennsylvania 19107
Principal Investigator: Joseph Abboud
Phone: 267-339-3566
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Philadelphia, PA
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Redwood City, California 94063
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Redwood City, CA
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Salisbury, Maryland 21804
Principal Investigator: Thomas A Brandon, M.D.
Phone: 410-749-4154
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Salisbury, MD
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