The Influence of Repairing the Sub-scapularis on Outcomes After Reverse Arthroplasty

Severe Arthropathy With a Grossly Deficient Rotator Cuff Clinical Trial

Official title:

A Prospective Multicenter Study to Examine the Influence of Repairing the Sub-scapularis on Outcomes After Reverse Arthroplasty: A Randomized, Controlled Trial.

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT03711175
• Other study ID #: PS-903
• Status: Enrolling by invitation
• Phase: N/A
• Start date: September 28, 2018
• Est. completion date: December 31, 2028

Study information

• Verified date: March 2022
• Source: Encore Medical, L.P.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is a prospective, multi-center, randomized blinded study to determine how repairing the subscapularis vs. not repairing the subscapularis when subjects are implanted with the AltiVate Reverse® Shoulder System for reverse total shoulder arthroplasty affects isometric and isokinetic internal rotational strength. It is hypothesized that patients in which the subscapularis is repaired will have improved postoperative isometric and isokinetic internal rotational strength.

Description:

Reverse shoulder arthroplasty (RSA) is performed to provide improvement in pain relief and restoration of function in patients with rotator cuff tear arthropathy and massive irreparable rotator cuff tears . Traditional total shoulder designs failed to address the unique mechanics of shoulders with deficient rotator cuffs. Different prosthesis designs exist for RSA, all of which increase the deltoid lever arm to provide a stable fulcrum for active elevation in a rotator cuff deficient shoulder. The Reverse® Shoulder Prosthesis (RSP®) (DJO Surgical) sought to address issues correlated to the Grammont design by lateralizing the center of rotation as well as utilizing a central compressive screw with a 5.0-mm peripheral locking screws for fixation and a glenosphere . Despite the success of the lateralized design, the effect of the repair of the subscapularis tendon during RSA on shoulder strength, range of motion, and shoulder function remains inconclusive. The rationale for repairing the subscapularis during RSA include anatomic preservation of a functioning rotator cuff muscle, an increased potential for internal rotation, better joint protection, and more stability. The reasoning for not repairing the subscapularis include that it may be biomechanically unfavorable for both the deltoid and the posterior rotator cuff, limiting the range of motion. As such, this randomized study aims to address if subscapularis repair impacts isometric and isokinetic internal rotational strength, with shoulder function and complications as secondary objectives, when patients are implanted with the AltiVate Reverse® device. The study will take place at multiple sites across the United States and will be managed by the DJO Surgical Clinical Affairs Department.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 200
• Est. completion date: December 31, 2028
• Est. primary completion date: December 31, 2028
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

1. Subject is =21 years of age

2. Subject is scheduled for reverse shoulder arthroplasty with the AltiVate Reverse device due to primary diagnosis of severe arthropathy with a grossly deficient rotator cuff

3. Subject's sub scapularis has been determined from MRI to be sufficient to repair

4. Subject is willing and able to comply with the study schedule and assessments

5. Subject is likely to be available for evaluation for the duration of the study

6. Subject is willing and able to sign the informed consent

Exclusion Criteria:

1. Subject is indicated for reverse shoulder arthroplasty for other indications (revision arthroplasty, proximal humerus fracture, etc.), addition of latissimus transfer or pectoralis major transfer

2. Subject has metal allergies or sensitivity

3. Subject has an active infection at or near the site of implantation

4. Subject has a nonfunctional deltoid muscle

5. Subject has neuromuscular compromise condition of the shoulder

6. Subject has known active metastatic or neoplastic diseases, Paget's disease or Charcot's disease

7. Subject is currently on or planning to be on chemotherapy or radiation

8. Subject has had chemotherapy or radiation within the last 6 months

9. Subject is currently taking > 5mg/day corticosteroids (e.g. prednisone), excluding inhalers, within 3 months prior to surgery

10. Female subjects who are pregnant or planning to become pregnant within the study period

11. In the investigator's opinion, the subject is unable to understand the study or be compliant with the follow up or has a history of non-compliance with medical advice

12. Subject has a history of any cognitive or mental health status that would interfere with study participation

13. Subject is abusing alcohol or drugs or is undergoing active treatment for substance abuse (e.g., recreational drugs, narcotics, or alcohol).

Related Conditions & MeSH terms

• Joint Diseases
• Severe Arthropathy With a Grossly Deficient Rotator Cuff

Intervention

Procedure:
• Subscapularis repair
Utilizing fiberwire, high tensile strength suture

Device:
• Shoulder implant
Reverse shoulder arthroplasty device

Locations

Country	Name	City	State
United States	Texas Orthopedic Group	Houston	Texas
United States	NYU Langone Center for Musculoskeletal Care	New York	New York
United States	Rothman Institute	Philadelphia	Pennsylvania
United States	St. Luke's Hospital	Saint Louis	Missouri

Sponsors (1)

Lead Sponsor	Collaborator
Encore Medical, L.P.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in isometric and isokinetic internal rotational strength of abductors	Maximal isometric strength of shoulder abductors and measured in kilograms using a force gauge	6 months, and 1, 2, 5 and 10 years
Primary	Change in isometric and isokinetic internal rotational strength of flexors	Maximal isometric strength of shoulder flexors measured in kilograms using a force gauge	6 months, and 1, 2, 5 and 10 years
Primary	Change in isometric and isokinetic internal rotational strength of internal rotators	Maximal isometric strength of shoulder measured internal rotators in kilograms using a force gauge	6 months, and 1, 2, 5 and 10 years
Primary	Change in isometric and isokinetic internal rotational strength of external rotators	Maximal isometric strength of shoulder measured external rotators in kilograms using a force gauge	6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in shoulder ROM with the AltiVate Reverse® Shoulder	Examine operative shoulder active forward elevation	6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in shoulder ROM with the AltiVate Reverse® Shoulder	Examine operative shoulder active abduction	6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in shoulder ROM with the AltiVate Reverse® Shoulder	Examine operative shoulder active external rotation	6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in shoulder ROM with the AltiVate Reverse® Shoulder	Examine operative shoulder active internal rotation	6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in shoulder functionality with the AltiVate Reverse® Shoulder	Examine change in ASES score	6 weeks,6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in shoulder functionality with the AltiVate Reverse® Shoulder	Examine change in pain per ASES assessment	6 weeks, 6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in shoulder functionality with the AltiVate Reverse® Shoulder	Examine change in SST score	6 weeks,6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in general health with the AltiVate Reverse® Shoulder	Examine change in VR-12	6 weeks, 6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate change in the radiographs of AltiVate Reverse® Shoulder	Examine radiographic parameters	6 weeks, 6 months, and 1, 2, 5 and 10 years
Secondary	To evaluate device survivorship of the AltiVate Reverse® Shoulder	Examine adverse events	6 weeks, 6 months, and 1, 2, 5 and 10 years