A Dynamic Elastic Garment (DEG) in Patients With Rotator Cuff Tendinopathy (DEG)
Primary Purpose
Rotator Cuff Tendinopathy
Status
Withdrawn
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Dynamic Elastic Garment (DEG) brace
Corticosteroid injection
Sponsored by
About this trial
This is an interventional treatment trial for Rotator Cuff Tendinopathy
Eligibility Criteria
Inclusion Criteria:
- Patient over 18 to 89 years of age with MRI-confirmed tendinosis of the rotator cuff (supraspinatus, infraspinatus, subscapularis, or teres minor tendons) with pain on clinical examination
- Symptomatic, nontraumatic rotator cuff tears as confirmed on MRI
Exclusion Criteria:
- Traumatic onset of shoulder symptoms
- Evidence of symptomatic glenohumeral osteoarthritis (osteophytes on plain films with pain or stiffness on examination)
- Partial or complete rotator cuff tears
- Previous surgery on the affected shoulder
- History of rheumatoid arthritis or other systemic inflammatory disorder
- Use of immunosuppressive therapies in the last 6 months
- Inability to comply with or properly document use of dynamic elastic garment for prescribed time.
Sites / Locations
- Loma Linda University Healthcare Department of Orthopaedic Surgery
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Dynamic elastic garment and injection
Corticosteroid injection
Arm Description
Outcomes
Primary Outcome Measures
Short Form-36
Short form Health questionnaire
Secondary Outcome Measures
Simple Shoulder Test
12 yes or no questions on function with the involved shoulder.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03032432
Brief Title
A Dynamic Elastic Garment (DEG) in Patients With Rotator Cuff Tendinopathy
Acronym
DEG
Official Title
A Single-blinded Randomized Controlled Trial Comparing Patients Who Receive a Corticosteroid Injection for Nontraumatic Degenerative Rotator Cuff Tears or Tendinopathy and Scheduled Use of a Dynamic Elastic Garment to Patients Who Receive a Corticosteroid Injection Alone.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Withdrawn
Why Stopped
Principle Investigator is no longer at Loma Linda University Medical Center
Study Start Date
June 12, 2018 (Actual)
Primary Completion Date
February 15, 2019 (Actual)
Study Completion Date
February 15, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Loma Linda University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine if patients with shoulder pain and MRI-confirmed rotator cuff tendinosis, will have their pain and function improved when treated with daily use of a dynamic elastic garment along with a corticosteroid injection, when compared to those patients who receive a corticosteroid injection alone. To our knowledge this is the first study to evaluate the use of a dynamic elastic garment on shoulders.
Group A: Control group, will receive and ultrasound-guided corticosteroid injection alone.
Group B: Intervention, ultrasound-guided corticosteroid injection and scheduled use of a dynamic elastic garment, by IntelliSkin.
Group C: Intervention corticosteroid injection and scheduled use of a Dynamic elastic garment, by AlignMed Posture Shirt 2.0.
Up to 60 patients will participate and be randomized in this study, both male and female between the ages of 18 to 89 years of age. Subjects will complete a few forms; SF-36, ASES, Simple Shoulder test, these will take place at the initial visit and Then again at your 4 week and 6 week visit.
This is a single center study, investigator initiated. 60 subjects will participate in the study at Loma Linda University.
Detailed Description
Shoulder pain is a common complaint with a reported prevalence of 7-26% in the general population(1). The most common etiology of shoulder pain in the primary care setting is rotator cuff disease (2-4), a term which encompasses several separate diagnoses. In an orthopaedic practice, rotator cuff disease includes tendinosis or tendinitis of the supraspinatus, infraspinatus, subscapularis, or teres minor tendons, subacromial impingement with or without bursitis, bicipital tendinitis, or a partial or complete rotator cuff tear. This study will specifically include patients with tendinosis or tendinitis of the rotator cuff, for which we will use the term rotator cuff tendinopathy.
There are myriad treatment options for rotator cuff tendinopathy; from conservative measures such as NSAIDs, corticosteroid injections, and physiotherapy to more invasive measures including arthroscopic decompression for subacromial impingement syndrome. While most orthopaedic surgeons will employ some combination of physiotherapy, NSAIDs, and corticosteroid injections for pain relief, the evidence supporting their efficacy in providing long-term pain relief and functional improvement is limited. Thus, there is clinical equipoise that exists when treating rotator cuff tendinopathy has led physicians to pursue other less traditional modalities. Some of these that have gained notoriety are hyperthermia, extracorporeal shock-wave treatment, electrotherapy modalities and more recently, non-elastic taping and elastic kinesiology taping.
Dynamic elastic garments are relatively new products which are being used to improve posture and provide shoulder and lumbar support. Abnormal scapular motion, particularly scapular protraction, has been shown to reduce the subacromial width and place undue strain on the rotator cuff. These garments utilize elastic bands placed in specific locations to provide postural support and proprioceptive feedback to the patient. This may help to restore normal shoulder kinematics and subsequently provide relief of shoulder symptoms.
Patients with MRI-confirmed tendinosis or tendinopathy of the rotator cuff will have improved shoulder pain relief and outcome scores when treated with scheduled use of a dynamic- elastic garment and a corticosteroid injection compared to those patients who receive a corticosteroid injection alone.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tendinopathy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Dynamic elastic garment and injection
Arm Type
Experimental
Arm Title
Corticosteroid injection
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
Dynamic Elastic Garment (DEG) brace
Other Intervention Name(s)
posture brace
Intervention Description
Improve function of the shoulder
Intervention Type
Drug
Intervention Name(s)
Corticosteroid injection
Intervention Description
Injection to improve rotator cuff tendinosis pain and functional score
Primary Outcome Measure Information:
Title
Short Form-36
Description
Short form Health questionnaire
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Simple Shoulder Test
Description
12 yes or no questions on function with the involved shoulder.
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
American Shoulder and Elbow Surgeons Shoulder Assessment (ASES)
Description
Shoulder Function questionnaire
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient over 18 to 89 years of age with MRI-confirmed tendinosis of the rotator cuff (supraspinatus, infraspinatus, subscapularis, or teres minor tendons) with pain on clinical examination
Symptomatic, nontraumatic rotator cuff tears as confirmed on MRI
Exclusion Criteria:
Traumatic onset of shoulder symptoms
Evidence of symptomatic glenohumeral osteoarthritis (osteophytes on plain films with pain or stiffness on examination)
Partial or complete rotator cuff tears
Previous surgery on the affected shoulder
History of rheumatoid arthritis or other systemic inflammatory disorder
Use of immunosuppressive therapies in the last 6 months
Inability to comply with or properly document use of dynamic elastic garment for prescribed time.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nirav H Amin, MD
Organizational Affiliation
Loma Linda University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loma Linda University Healthcare Department of Orthopaedic Surgery
City
Loma Linda
State/Province
California
ZIP/Postal Code
92354
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
A Dynamic Elastic Garment (DEG) in Patients With Rotator Cuff Tendinopathy
We'll reach out to this number within 24 hrs