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NCT Number: NCT06319911

AETOS Shoulder System

The goal of this study is to confirm the safety and performance of the AETOS Shoulder System for USA adoption. This is a prospective, open, adaptive, non-comparative, multi-centre investigation enrolling a maximum of 220 subjects in 2 cohorts (anatomic and reverse) at up to 15 sites. No intra-study comparator group will be included, and there will be no randomization

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Key information

Conditions

Shoulder Osteoarthritis Shoulder Arthritis

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

California Pacific Orthopedics, San Francisco, California, United States

Loading trial locations.

About this study

This study will confirm the safety and performance of the AETOS Shoulder System in anatomic and reverse TSA. Revisions will not be enrolled into this study.

The AETOS Shoulder System is manufactured by Smith & Nephew, Inc., 1450 Brooks Road Memphis, Tennessee 38116 USA, and has been 510k Cleared as of 07Jun2023; therefore, it is considered a post-market product and will be procured through normal commercial channels in the USA. The humeral stem is designed to be used for both Total Shoulder Arthroplasty (TSA) and reverse shoulder arthroplasty procedures. The humeral stems are designed with fins and a porous plasma coating to provide fixation within the proximal humeral metaphysis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients must meet all the following criteria to be included in the study:

  • Patient is at least 18 years of age at the time of consent and skeletally mature.
  • Patient is undergoing a primary elective anatomic or reverse shoulder replacement surgery for one of the following indications:
  • Rheumatoid arthritis, and/or
  • Traumatic arthritis (Post Traumatic arthritis), and/or
  • Non-inflammatory degenerative joint disease, and/or
  • Correction of functional deformity.
  • Patient is willing and able to accommodate all study-related procedures and visits detailed in the protocol & cooperate in the standard of care post-operative therapy.
  • Patient is geographically stable and willing to return to the study site for all follow-up visits.
  • Patient has been adequately informed of risks and requirements of the study and is willing and able to provide informed consent for participation.

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Exclusion criteria

Patients who meet any of the following criteria will not qualify for participation in the trial:

  • Patient has a contraindication to AETOS.
  • Patient is undergoing a revision shoulder replacement surgery including total or partial arthroplasty.
  • Patient is indicated for a Hemiarthroplasty.
  • Patient has traumatic injury or a fracture.
  • Patient has uncontrolled diabetes with a hemoglobin A1C of 7.5 or greater.
  • Patient has comorbidities/conditions that preclude proper healing/fixation of the implant.
  • Patient has poor quality or insufficient bone stock to support the implant.
  • Patient has poor bone quality where there could be considerable migration of the implant and/or a chance of fracture.
  • Patient has rapid joint destruction, marked bone loss or bone resorption (e.g., severe osteoporosis).
  • Patient has osteomalacia.
  • Patient has muscular, neurologic, or vascular deficiencies that may compromise the outcome of the shoulder replacement surgery.
  • Patient has a known sensitivity, allergic reaction, and/or known allergies to one or more of the implanted materials.
  • Patient has a distant foci of infection which may spread to the implant site, active local or systemic infection, sepsis, or osteomyelitis.
  • Patient has an elevation of sedimentation rate, elevation of WBC count, or marked shift in WBC differential count unexplained by other disease.
  • If reverse shoulder arthroplasty, patient has a non-functional deltoid or external rotator muscles.
  • If reverse shoulder arthroplasty, patient has a significant injury to the upper brachial plexus.
  • If reverse shoulder arthroplasty, patient has paralysis of the axillary nerve.
  • Patient is uncooperative, has a neurologic disorder and is not capable of following directions, or is a vulnerable subject per ISO 14155 (i.e., individuals who are unable to fully understand all aspects of the investigation that are relevant to the decision to participate, or who could be manipulated or unduly influenced as a result of a compromised position, expectation of benefits or fear of retaliatory response).
  • Patient is pregnant or plans to become pregnant during the follow-up period.
  • Patient has a Body Mass Index (BMI) of >35kg/m2 or a BMI that may compromise the outcome of the shoulder replacement surgery.
  • Patient has anticipated activities which would impose high stresses on the implant and its fixation or has a high likelihood of a fall.
  • Patient is a known smoker, vaper, alcohol abuser, or drug abuser within 180 days of consent.
  • Patient has participated previously in this clinical trial and was withdrawn.
  • Patient is participating in another device or drug trial or observational competitive study.

Treatment and study plan

AETOS

Device

The AETOS Shoulder System will be implanted into the right or left shoulder in the anatomic or reverse configuration

Primary outcomes

  1. Implant Survivorship

    Time frame: 2 years

    Implant survivorship at 2 years post operatively defined as absence of device removal or revision of any component

Secondary outcomes

  1. Implant Survivorship at 6 months, 1 year, 3.5 years and 5 years

    Time frame: 6 months, 1 year, 3.5 years, and 5 years

    Implant Survivorship at 6 months, 1 year, 3.5 years, and 5 years defined as absence of device removal or revision of any component

  2. Radiographic Assessment - Glenoid Migration/Subsidence

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Glenoid Component Migration / Subsidence collected post-surgery at day 0, 1 year, 2 years, and 5 years will be graded in accordance with the following definitions:

    • Absent: No evidence of glenoid component displacement ≥ 5 mm relative to the native bone stock.
    • Present: Presence of glenoid component displacement ≥ 5 mm relative to the native bone stock.

  3. Radiographic Assessment - Glenoid Radiolucency

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Glenoid Component Radiolucency - antero-posterior (AP) collected post-surgery at day 0, 1 year, 2 years, and 5 years will be graded in accordance with the following definitions:

    • Absent: No evidence of radiolucency > 2 mm in width along the bone-implant / bone-cement interface in any zone.
    • Present: Presence of radiolucency > 2 mm in width along the bone-implant / bone-cement interface in one or more zones.

  4. Radiographic Assessment - Humeral Radiolucency

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Humeral Component Radiolucency - AP collected post-surgery at day 0, 1 year, 2 years, and 5 years will be graded in accordance with the following definitions:

    • Absent: No evidence of radiolucency > 2 mm in width along the bone-implant interface in any zone.
    • Present: Presence of radiolucency > 2 mm in width along the bone-implant interface in one or more zones.

  5. Radiographic Assessment - Humeral Migration/Subsidence

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Humeral Component Migration / Subsidence collected post-surgery at day 0, 1 year, 2 years, and 5 years will be graded in accordance with the following definitions:

    • Absent: No evidence of a change in position of the humeral component relative to the native bone stock ≥ 5 mm.
    • Present: Presence of a change in position of the humeral component relative to the native bone stock ≥ 5 mm

  6. Radiographic Assessment - Humeral Head Centeredness

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Humeral Head Centeredness collected post-surgery at day 0, 1 year, 2 years, and 5 years will be calculated using the method described by Iannotti and Norris from the axillary view

  7. Radiographic Assessment - Bone Remodeling

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Bone Remodeling of the humerus collected post-surgery at day 0, 1 year, 2 years, and 5 years will be graded in accordance with the following definitions by Schnetzke et al.:

    • Absent: No evidence of humerus bone remodeling.
    • Present: Presence of one or more features of humerus bone remodeling.
    • 1. Condensation Lines: Presence of condensation lines around the tip of the stem.
    • 2. Cortical Thinning: Presence of cortical thinning and osteopenia.
    • 3. Spot Welds: Presence of spot welds.
    • 4. Other: Other feature not listed above.

  8. Radiographic Assessment - Glenohumeral Subluxation

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Glenohumeral Subluxation collected post-surgery at day 0, 1 year, 2 years, and 5 years will be will be derived from the Humeral Head Centeredness assessment using the following definitions, from Iannotti and Norris et al.:

    • Absent: Humeral Head Centeredness is ≤25%.
    • Present: Humeral Head Centeredness is >25%.

  9. Radiographic Assessment - Device Condition: Anatomic

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Device Condition - Anatomic collected post-surgery at day 0, 1 year, 2 years, and 5 years will be graded in accordance with the following definitions:

    • Intact: No evidence of fracture, breakage, loosening, disassembly or migration of any of the components of the anatomic AETOS TSA.
    • Not Intact: Presence of fracture, breakage, loosening, disassembly or migration of one or more of the components of the anatomic AETOS TSA:
    • 1. Humeral Stem.
    • 2. Humeral Head.
    • 3. Glenoid.
    • 4. Post Extension.

  10. Radiographic Assessment - Device Condition: Reverse

    Time frame: Day 0, 1 year, 2 years, and 5 years

    Device Condition - Reverse collected post-surgery at day 0, 1 year, 2 years, and 5 years will be graded in accordance with the following definitions:

    • Intact: No evidence of fracture, breakage, loosening, disassembly or migration of any of the components of the reverse AETOS TSA.
    • Not Intact: Presence of fracture, breakage, loosening, disassembly or migration of one or more of the components of the reverse AETOS TSA:
    • 1. Humeral Stem.
    • 2. Reverse Liner.
    • 3. Glenosphere.
    • 4. Metal Glenoid.
    • 5. Peripheral Screws.
    • 6. Central Screw.
    • 7. Humeral Spacer.
    • 8. Post Extension.

  11. American Shoulder and Elbow Score (ASES)

    Time frame: 6 months, 1 year, 2 years, and 5 years

    The ASES instrument is composed of 2 sections containing participant self-reported and clinician assessments. The ASES score is a 0 to 100-point rating with a higher score indicating improvement in pain and function.

  12. Constant Murley Score

    Time frame: 6 months, 1 year, 2 years, and 5 years

    Constant-Murley Shoulder (CMS) scale assesses four aspects related to shoulder pathology; two subjective: pain and activities of daily living (ADL) and two objective: range of motion (ROM) and strength. The subjective components can receive up to 35 points and the objective 65, resulting in a possible maximum total score of 100 points (best function). Pain and ADL are answered by the subject; ROM and strength require a physical evaluation and are answered by the orthopaedic surgeon or the physiotherapist.

  13. Simple Shoulder Test (SST)

    Time frame: 6 months, 1 year, 2 years, and 5 years

    Series of 12 "yes" or "no" questions the patient answers about the function of the involved shoulder. The answer to these questions provides a standardized way of recording the function of a shoulder before and after treatment.

  14. Single Assessment Numeric Evaluation (SANE)

    Time frame: 6 months, 1 year, 2 years, and 5 years

    The SANE is a simple, single-question, patient-based shoulder function assessment tool: ''How would you rate your shoulder today as a percentage of normal (0% to 100% scale with 100% being normal)?''

Study contacts

Contact information is provided by the study sponsor or research team.

Karlie Morgan

CONTACT

[email protected]

5124967507

Tammy Clark, MPH

CONTACT

[email protected]

3512269585

Sponsors and collaborators

Lead sponsor

Smith & Nephew, Inc.

Industry

Registry information

Official study title

AETOS Shoulder System Post Market Clinical Investigation

Important dates

Study start
2024
Primary completion
2027
Study completion
2030
First posted
Mar 20, 2024
Registry last updated
May 7, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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