Reverse Shoulder Prosthesis Prospective Multi-Center Study

Sponsor
Encore Medical, L.P. (Industry)
Overall Status
Completed
CT.gov ID
NCT01005446
Collaborator
DJO Incorporated (Industry)
245
10
102
24.5
0.2

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the use and efficacy of the Reverse® Shoulder Prosthesis for treatment of rotator cuff deficiency in subjects who are candidates for a total shoulder replacement (primary and revision subjects).

Condition or Disease Intervention/Treatment Phase
  • Device: Encore Reverse Shoulder Prosthesis (RSP®)

Detailed Description

Reverse shoulder arthroplasty for the treatment of rotator cuff deficiency and glenohumeral arthritis have shown favorable outcomes in pain and function over the short and medium term. A prospective, multi-center study on the outcomes of subjects treated with the RSP would be a valuable addition to the literature and give important information regarding an ever-increasing treatment option for subjects with rotator cuff deficiency. The study will take place at multiple sites across the United States and will be managed by the DJO Surgical Clinical Affairs Department. The study will include only subjects who meet the indications for use criteria for the Reverse® Shoulder Prosthesis and who are candidates for total shoulder replacement surgery.

Study Design

Study Type:
Observational
Actual Enrollment :
245 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
PS-901: Prospective Multicenter Open Label Study of the Encore Reverse® Shoulder Prosthesis
Study Start Date :
Dec 1, 2009
Actual Primary Completion Date :
Aug 1, 2017
Actual Study Completion Date :
Jun 1, 2018

Arms and Interventions

Arm Intervention/Treatment
RSP Device

Post Market Study

Device: Encore Reverse Shoulder Prosthesis (RSP®)
The RSP is indicated for use in subjects with grossly rotator cuff deficient shoulder joints with severe arthropathy or a previously failed joint replacement with a grossly rotator cuff deficient shoulder joint.
Other Names:
  • RSP®
  • Outcome Measures

    Primary Outcome Measures

    1. Improvement in American Shoulder and Elbow Surgeons Score (ASES) from Baseline [2 year]

      Improvement in American Shoulder and Elbow Surgeons Score (ASES) from Baseline. Assessments include: 1) Pain score where 0=no pain at all and 10=pain as bad as it can be 2) Function score where 0=my should is useless and 10=my shoulder is normal 3) Activity score where 0=unable to do and 3=Normal.

    Secondary Outcome Measures

    1. Radiologic Success [5 year]

      Changes in radiolucency compared with Baseline

    2. Change in ASES score from Baseline [5 year]

      Improvement in American Shoulder and Elbow Surgeons Score (ASES) from Baseline. Assessments include: 1) Pain score where 0=no pain at all and 10=pain as bad as it can be 2) Function score where 0=my should is useless and 10=my shoulder is normal 3) Activity score where 0=unable to do and 3=Normal.

    3. SF36- (Short Form 36)Health Survey [5 year]

      Change from baseline using the SF36-Health Status. There are multiple scales for general health, pain and activities of daily living

    4. Change in Simple Shoulder Test from Baseline [5 year]

      Change in Simple Shoulder Test from Baseline. Twelve questions about pain and functionality with responses being yes or no

    5. Subject Satisfaction Survey [5 year]

      Patient Related Outcome of Device Satisfaction (score 1-5 with 1 = best and 5 = worst) Device satisfaction

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    60 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Subject must be a candidate for a total shoulder joint replacement

    • Subject must be diagnosed with one or more of the following conditions:

    Irreparable rotator cuff tear with gleno-humeral arthritis; Failed rotator cuff surgery with gleno-humeral instability or antero- superior escape; Failed shoulder replacement surgery

    • Subject has a functional deltoid muscle

    • Subject's joint must be anatomically and functionally suited to receive the selected implant

    • Subject is 60 years of age or older (≥ 60 yrs of age) at time of consent

    • Subject is likely to be available for all study visits

    • Subject is able and willing to sign the informed consent and follow study procedures

    • Subject is not pregnant

    Exclusion Criteria:
    • Subject has a non-functional deltoid muscle

    • Subject has a mental condition(s) that may interfere with the subject's ability to give an informed consent or willingness to fulfill the study requirements (i.e., severe mental retardation such that the Subject cannot understand the informed consent process, global dementia, prior strokes that interfere with the Subject's cognitive abilities, senile dementia, and Alzheimer's Disease)

    • Subject is a prisoner

    • Subject has high levels of physical activity (ex. competitive sports, heavy physical labor)

    • Subject is pregnant

    • Subject has an active infection or sepsis

    • Subject has loss of ligamentous structures

    • Subject has a history of alcoholism or other addictions (current or past)

    • Subject has muscular, neurological or vascular deficiencies which compromise the affected extremity (i.e., Parkinson's Disease, Syringomyelia and Multiple Sclerosis, Charcot joints)

    • Subject has severe glenoid bone loss

    • Subject has known materials sensitivity (to metals)

    • Subject is younger than 60 years of age (< 60 years of age) at consent

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Stanford University - Dept. of Orthopedics Redwood City California United States 94063
    2 Coastal Orthopedics & Sports Medicine Bradenton Florida United States 34209
    3 Orthopaedic Institute at Holy Cross Hospital Fort Lauderdale Florida United States 33334
    4 Rush-Presbyterian-St. Luke's Medical Center Chicago Illinois United States 60612
    5 Norton Orthopaedic & Sports Medicine Specialists Louisville Kentucky United States 40241
    6 Excelsior Orthopaedics Amherst New York United States 14226
    7 Cincinnati Sports Medicine and Orthopeadic Center Cincinnati Ohio United States 45242
    8 Geisinger Medical Center Danville Pennsylvania United States 17822
    9 Texas Center for Joint Replacement Plano Texas United States 75093
    10 Rimrock Orthopedics Saint George Utah United States 84790

    Sponsors and Collaborators

    • Encore Medical, L.P.
    • DJO Incorporated

    Investigators

    • Principal Investigator: Samer S. Hasan, M.D., Cincinnati Sports Medicine and Orthopaedic Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Encore Medical, L.P.
    ClinicalTrials.gov Identifier:
    NCT01005446
    Other Study ID Numbers:
    • PS - 901
    First Posted:
    Nov 1, 2009
    Last Update Posted:
    Mar 30, 2021
    Last Verified:
    Mar 1, 2021
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 30, 2021