Shoulder Pain, Shoulder Impingement Syndrome, Rotator Cuff Tendinitis
Conditions
Brief summary
DJO UK Ltd (ENOVIS) is conducting this study to assess the effectiveness of LightForce® Therapy Lasers on pain reduction in shoulder soft tissue inflammation. In detail this study will assess superiority of LightForce® Therapy Lasers combined with standard of care, represented by physiotherapy/exercise program compared to sham laser combined with standard of care (physiotherapy/exercise program) on pain reduction in subjects with shoulder soft tissue inflammation due to Impingement (Subacromial impingement syndrome (SAIS)) or Rotator Cuff Tendinopathy (RCT),. In addition, this study allows to collect post market clinical data on the safety and performance of LightForce® Therapy Lasers, when used, following the normal clinical practice, in accordance with its approved and CE marked intended use.
Detailed description
This clinical investigation is a post-market, International, multi center, prospective, randomized, sham controlled, single blind study to assess the effectiveness of LightForce® Therapy Lasers and to collect PMCF data on the safety and performance of LightForce® Therapy Lasers, when used in accordance with its approved labeling, to comply with Medical Device Regulation (EU) 2017/745 (MDR) Article 61 and Part B of Annex XI.
Interventions
DEVICESham Laser therapy
sham laser therapy for 4 consecutive weeks with a minimum of 3 sessions per week.
DEVICELaser therapy
laser therapy for 4 consecutive weeks with a minimum of 3 sessions per week.
OTHERphysiotherapy/exercise protocol
physiotherapy/exercise protocol represents the standard of care (SOC) and the program includes Codman's pendulum exercise, range of motion (ROM) exercises, stretching and isometric strengthening exercises, for 4 consecutive weeks with a minimum of 3 sessions per week.
Sponsors
Donawa Lifescience Consulting
DJO UK Ltd
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patient male or female with age ≥18 years old 2. Patient with diagnosis of shoulder soft tissue inflammation due to SAIS/RCT (as confirmed by physical examination and/or imaging) to be treated by LightForce® Therapy Lasers according to its indications. 3. Patient suffering from shoulder soft tissue inflammation due to SAIS/RCT pain for more than 3 months prior to enrollment 4. Pain (either persistent or during activities) score reported by the subject at baseline ≥ 40 mm measured on VAS 5. Patient able to provide written informed consent
Exclusion criteria
1. Patient with musculoskeletal pathological conditions not to be treated with/contraindication to the use of LightForce® Therapy Lasers according to its intended use and indications 2. Patients who are taking drugs that have heat or light sensitive contraindications, such as but not limited to certain types of steroids 3. Patients who are administered with corticosteroids, should discontinue the treatment at least 2 weeks prior to study treatment start 4. Pregnant females or females of childbearing potentially planning to become pregnant during the study participation 5. Patients who had systemic inflammatory conditions (i.e.rheumatoid arthritis, polymyalgia rheumatica) 6. Patients who underwent intra-articular injection (Ialuronic acid, platelet rich plasma or corticosteroids) in the shoulder in the last 3 months 7. Patients who have a disease that would limit their participation in exercises (i.e. severe chronic obstructive pulmonary disease, severe heart failure, cerebrovascular event history) 8. Patients with a prior history of surgical intervention and implantation of a metal implant into the affected shoulder 9. Patients with a diagnosis of active cancer 10. Patients with tattoos covering more than 30% of the area to be treated with LightForce® Therapy Lasers 11. Patients who are mentally or physically incapacitated 12. Patient participating in other clinical study or has completed a clinical study less than 30 days prior to enrollment 13. Patient affected by shoulder soft tissue acute inflammation due to recent sport injury or trauma 14. Patients with other musculoskeletal problems of the shoulder joint such as calcifying tendinitis, full thickness rotator-cuff tear, adhesive capsulitis, fibromyalgia, recent surgery or fracture of the shoulder joint, and/or undergoing to specific physiotherapy for these (recent is defined as within 30 days prior to enrollment). 15. Patients with other clinically significant co-morbidities that make the patient unsuitable for study participation, at the discretion of the investigator
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain change | 4 weeks after treatment start | Pain reduction measured with Visual Analog Scale (VAS) (in a scale 0-100 mm, where 0 is no pain and 100 is the worst possible pain) after 4 weeks of treatment compared to pre-treatment (baseline) VAS |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Safety - adverse event rate | through study completion, an average of 21 weeks | Proportion of patient experiencing an adverse event associated with device use |
Other
| Measure | Time frame | Description |
|---|---|---|
| Patient overall status change | 2, 4, 6 ans 12 weeks after treatment start | Patient ratings of overall improvement, assessed by QoL (SF-12): The SF-12 is a self-reported outcome measure assessing the impact of health on an individual's everyday life. The SF-12 uses 12 items and scores range from 0 to 100, with higher scores indicating better physical and mental health functioning. SF-12 will be assessed at 2, 4, 6 weeks and at 12 weeks and compared to baseline |
| Range of motion (ROM) for shoulder | 2, 4, 6 ans 12 weeks after treatment start | Range of motion for shoulder both passive and active, pain free and at maximum ROM, in all the planes of motion, measured by a universal goniometer at2, 4, 6 ans 12 weeks after treatment start compared to baseline |
| Neer test | 2, 4, 6 ans 12 weeks after treatment start | Functional test to assess shoulder pain onset at a certain degree of movement during flexion and pressure application (often used as a diagnositc tool of subacromial impingement) performed at 2,4, 6 and at 12 weeks after treatment start and compared to baseline |
| Pain change | 1,2,3,6, 9 and 12 weeks | Pain measured with Visual Analog Scale (VAS) (in a scale 0-100 mm, where 0 is no pain and 100 is the worst possible pain) at 1,2,3,6, 9 and 12 weeks after treatment start to assess short-term and long-term pain management compared to baseline |
| Jobe test | 2, 4, 6 ans 12 weeks after treatment start | Functional testing of the arm with the thumb in 'thumbs up' and resistance provided by the examiner, weakness or pain would represent a positive test indicating a tear of the supraspinatus muscle or tendon, it will be performed at 2,4, 6 and at 12 weeks after treatment start and compared to baseline |
| Rate of patients needed new treatment | 18 weeks after treatment start | Patients will be asked through a questionnaire whether any new treatment and in case which one (pharmacological, physiotherapic etc) was needed to manage shoulder pain after 12 weeks from treatment start |
| Palm up test | 2, 4, 6 ans 12 weeks after treatment start | Functional test where the patient elevates the extended arm with the palm facing upwards and against examiner's resistance, presence of pain can denote tendonitis (often used as diagnostic tool) and performed at 2,4, 6 and at 12 weeks after treatment start and compared to baseline |
| Shoulder pain and disability | 2, 4, 6 and at 12 weeks | Shoulder pain and disability measured with the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire (the score output is given as a percentace -from 0% to 100%- and the lower the percentage the better is the clinical outome, the higher the percentage the worse is the clinical outcome) performed at 2, 4, 6 and at 12 weeks after treatment start compared to baseline. |
Countries
France, Italy, United Kingdom
Contacts
Primary ContactElena Arcangeli
Outcome results
None listed