PEMF as Adjunctive Treatment Following Surgical Repair of Full Thickness Rotator Cuff Tears

NCT ID: NCT03339492

Last Updated: 2023-08-30

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 377 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-01-15
• Study Completion Date: 2022-12-31

Brief Summary

The primary objective of this study is to prospectively determine, at 12 months post-surgical repair of full thickness rotator cuff tears, the safety and efficacy of treating full thickness rotator cuff repairs with pulsed electromagnetic fields (PEMF). The hypothesis states that exposure to a pulsed electromagnetic field (PEMF) following surgical repair of a full thickness rotator cuff tendon tear reduces tendon re-tear rates. The strength of the shoulder muscles and the levels of pain in subjects after surgical repair of their rotator cuff adjunctively treated with an active PEMF device will also be measured.

Detailed Description

This Clinical Investigation Plan (CIP) describes the prospective, randomized, double-blind, placebo controlled study to evaluate the safety and efficacy of Pulsed Electromagnetic Field (PEMF) therapy as an adjunctive treatment to surgical repair of full thickness rotator cuff tears.

Rotator cuff tears are common musculoskeletal injuries which often require surgical intervention. Unfortunately, post-repair prognosis is poor, and surgical repairs have been reported to fail in up to 94% of cases (Galatz et. al., 2004). Repaired tissue tends to be fibrotic, disorganized, and reattaches poorly to the bony insertion. To improve tendon-to-bone healing, many non-invasive therapeutic devices have been utilized post-operatively including therapeutic ultrasound and shock wave therapy (Lovric et. al., 2013; Springer and Badgett, 2015).

In orthopedics, the use of these non-invasive therapeutic devices has become increasingly popular during the post-operative recovery period in an effort to enhance tissue healing. These devices are relatively inexpensive and easily obtainable and relatively easy to use, and are especially enticing as they can be brought into the patient's home and do not require frequent visits to the clinic. Additionally, non-invasive therapeutic devices can be used for a variety of applications, including promoting tissue healing prior to surgical intervention or in lieu of surgical intervention all together. Although there are numerous advantages to using non-invasive therapeutic devices, their efficacy has not yet been maximized.

Based on the pre-clinical work presented (Tucker et. al., 2016; Huegel et. al., 2017), it is believed that pulsed electromagnetic fields may be an effective adjunctive treatment for patients who have undergone surgical repair of a torn rotator cuff.

Conditions

Full-thickness Rotator Cuff Tear

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Active PEMF

Subjects have 2 out of 3 chance to get the active device which emits a pulsed electromagnetic field (PEMF) from the RCStim Model 1114 device (right and left side models available). Double-blind randomization.

Group Type: ACTIVE_COMPARATOR

RCStim Model 1114

Intervention Type: DEVICE

Active device emits PEMF signal; placebo/control device does not emit PEMF signal

Control/placebo PEMF

Subjects have a 1 out of 3 chance to get the control/placebo device which does not emit a pulsed electromagnetic field (PEMF) from the RCStim Model 1114 device (right and left side models available). Double-blind randomization.

Group Type: SHAM_COMPARATOR

RCStim Model 1114

Intervention Type: DEVICE

Active device emits PEMF signal; placebo/control device does not emit PEMF signal

Interventions

RCStim Model 1114

Active device emits PEMF signal; placebo/control device does not emit PEMF signal

Intervention Type: DEVICE

Other Intervention Names

Orthofix rotator cuff soft tissue stimulator

Eligibility Criteria

Inclusion Criteria

1. Subject may be male or female between 21 years of age and 80 years of age at the time of consent.

2. Subject must have a repairable (≥1 and ≤ 5 cm in the AP direction) full thickness tear of either the supraspinatus tendon or both the supraspinatus and infraspinatus tendons, as determined by MRI and confirmed intra-operatively (pre-debridement) during the surgical repair of the rotator cuff using a calibrated probe.

a. Subjects who do not meet this criterion will be considered screen failures.

3. This must be the first rotator cuff repair surgery on the study shoulder with the following exceptions:

1. Previous repairs of the teres minor and/or the subscapularis muscles are permitted.

2. Previous acromioplasties, decompressions, and clavicular fracture repairs are permitted.

3. Concurrent acromioplasties, subacromial decompressions and/or distal clavicular excisions are permitted.

4. Concurrent fracture repairs or reconstructions are NOT permitted.

5. Biceps tenodesis or tenotomy (open or closed) are permitted.

4. Subject must not have used NSAIDs for one (1) week prior to surgery.

5. Subjects must agree NOT to use NSAIDS suring the first 6 weeks of the study. Low dose aspirin (81 mg) is permitted.

6. Subject must be willing and able to participate in post-operative physical therapy exercises.

7. Subject must be willing and able to follow all study procedures and return for all study visits.

8. Subject must have reliable access to any iOS device using iOS v.9.3 or later or an Android device with WiFi access for downloading the free device-specific app.

9. Subject must understand and be willing to sign the IRB-approved Informed Consent Document.

Exclusion Criteria

1. Subject has a tear <1cm or >5cm in size measured intraoperatively, pre-debridement, using a calibrated probe.

a. Subjects who do not meet this criterion will be considered screen failures.

2. Subject has a BMI > 45.

3. Subject has a pacemaker or defibrillator.

4. Subject is not able to or is unwilling to have an MRI on the study shoulder.

5. Subject requires assistive devices to walk such as crutches or walkers.

6. Subject has a rotator cuff tear in which the subscpularis tendon requires repair.

a. Biceps tenodesis or tenotomy (open or closed) is allowed.

7. Subject has a Fuchs score grade of 3 for fatty infiltration on any of the rotator cuff muscles.

Grade 1: Normal muscle, no or some fatty streaks Grade 2: Moderately pathologic muscle; more muscle than fat Grade 3: Advanced degeneration; as much muscle as fat or less muscle than fat

8. Subject has moderate to severe arthritis based on preoperative imaging or as judged at the time of arthroscopy.

1. Pre-operative x-ray findings consistent with Grade 3 or Grade 4 glenohumeral arthritis, where the grades are defined as follows:

Grade 1: doubtful narrowing of joint space and possible osteophytic lipping; Grade 2: definite osteophytes and definite narrowing of joint space; Grade 3: moderate multiple osteophytes and definite narrowing of joint space and some sclerosis and possible deformity of bone contour.

Grade 4: bone on bone morphology

2. Intra-operative exposed subchondral bone involving >= 50% of either the humeral head, glenoid or both.

9. Subject has a known collagen disorder such as, but not limited to, osteogenesis imperfecta (OI) or Ehlers-Danlos syndrome (EDS).

10. Subject has a known inflammatory or autoimmune connective tissue disease such as, but not limited to, gout affecting the shoulder, scleroderma, SLE, rheumatoid disease, or calcific tendonitis of the shoulder.

11. Subject has a metabolic bone disease such as Paget's disease or osteomalacia.

a. Subjects with osteoporosis are not excluded from the study.

12. Subject has a deltoid defect, deltoid palsy or any other pseudoparalysis.

13. Subject has HIV, hepatitis, or has had an active malignancy in the past 5 years.

14. Subject has had previous rotator cuff repairs or repairs of the labrum.

a. See Inclusion Criterion #3 for permitted surgeries.

15. Subject has a diagnosis of fibromyalgia or other chronic pain syndrome.

16. Subject has shoulder pain of unknown etiology.

17. Subject has an active or on-going neoplastic disease, except for benign skin cancer(s).

18. Subject has undergone administration, within the last 30 days, of any type of corticosteroid (with the exception of asthma medications and ophthalmic medications), antineoplastic, immunostimulation or immunosuppressive agent.

19. Subject is septic or has a local or systemic infection.

20. Subject has an admitted active substance abuse problem which includes recreational drugs and/or narcotics or a history of substance abuse where history is defined as "not under the care of a physician" for more than 5 years.

a. Prescriptive medical marijuana is not permitted, including CBD oils.

21. Subject consumes more than 14 (men) or 7 (women) standard drinks (alcoholic units) per week where a drink equals a 12 oz. beer, or a 5 oz. glass of wine, or a 1.5 oz. shot of liquor.

22. Subject is currently seeking or receiving worker's compensation for this injury or for an injury that has occurred more than12 months prior to enrollment in this study or subjects who are currently in litigation or who have a history of litigation related to musculoskeletal diagnoses.

23. Subject has a major mental illnesses including major depression, bipolar disorder, schizophrenia or dementia that would prevent them from following the protocol and/or independently completeing the patient reported outcomes measures.

24. Subjects who have coexistent cervical spinal pathologies such as radiculopathies or myelopathies.

25. Subject has a mental or physical condition that would prevent tem from complying with the study protocol.

26. Subject has any other condition that, in the opinion of the investigator, would prevent them from completing the study.

27. Subject is a prisoner.

28. Subject has participated in another clinical trial within the last 90 days. a. The last study visit attended by the subject starts the 90 day window.

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Orthofix Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

The CORE Institute

Phoenix, Arizona, United States

Stanford University

Redwood City, California, United States

UCSF Orthopedics

San Francisco, California, United States

Sabesan Orthopedics Research

Atlantis, Florida, United States

Coastal Orthopedics and Sports Medicine

Bradenton, Florida, United States

Holy Cross Hospital

Fort Lauderdale, Florida, United States

Andrews Institute

Gulf Breeze, Florida, United States

Cleveland Clinic Florida

Weston, Florida, United States

Rush University Medical Center

Chicago, Illinois, United States

Univ. of Maryland Dept of Orthopedics

Baltimore, Maryland, United States

Sinai Hospital of Baltimore

Baltimore, Maryland, United States

Univ of Michigan Orthopedic Sports Medicine Program

Ann Arbor, Michigan, United States

Univ Orthopedics Associates at Great Neck

Great Neck, New York, United States

Wake Forest Baptist Health

Winston-Salem, North Carolina, United States

Cincinnati Sports Medicine

Cincinnati, Ohio, United States

Univ. of Pennsylvania Orthopedics

Philadelphia, Pennsylvania, United States

The Rothman Institute

Philadelphia, Pennsylvania, United States

University Orthopedics Center

State College, Pennsylvania, United States

South Carolina Sports Medicine and Orthopedics

North Charleston, South Carolina, United States

The Campbell Clinic

Germantown, Tennessee, United States

Deutsch Shoulder

Houston, Texas, United States

Atlantic Orthopedics

Virginia Beach, Virginia, United States

Jordan-Young Research Institute

Virginia Beach, Virginia, United States

Countries

United States

Other Identifiers

CP-1604PSRC

Identifier Type: -

Identifier Source: org_study_id