Treatment of Chronic Shoulder Pain in Persons With Spinal Cord Injury Using Injection With Autologous Micro-Fragmented Adipose Tissue Under Ultrasound Guidance
Overview
- Phase
- Early Phase 1
- Intervention
- Not specified
- Conditions
- Shoulder Pain
- Sponsor
- Kessler Foundation
- Enrollment
- 10
- Locations
- 1
- Primary Endpoint
- Numerical Rating Scale
- Last Updated
- 6 years ago
Overview
Brief Summary
Rotator cuff disease (i.e., rotator cuff tendinopathy or tear) is a common cause of shoulder pain in persons with chronic spinal cord injury (SCI). It usually resolves with non-operative treatments such as pharmacological agents and physical therapy; however, when this fails, rotator cuff surgery may be the only option. Autologous adipose tissue injection has recently emerged as a promising new treatment for joint pain and soft tissue injury. Adipose can be used to provide cushioning and filling of structural defects and has been shown to have an abundance of bioactive elements and regenerative perivascular cells (pericytes). The purpose of this study is to explore the safety and efficacy of autologous, micro-fragmented adipose tissue (Lipogems®) injection under ultrasound guidance for chronic shoulder pain in persons with SCI.
Detailed Description
This is an exploratory pilot study to determine the safety and efficacy of autologous, micro-fragmented adipose tissue (Lipogems®) injection under ultrasound guidance for chronic, nonresponsive shoulder pain due to rotator cuff disease (i.e., rotator cuff tendinopathy) in persons with spinal cord injury (SCI). Twelve (12) persons with SCI who have chronic shoulder pain for longer than 6 months in spite of completing conservative treatment who are diagnosed with rotator cuff disease on examination. Micro-fragmented adipose tissue will be obtained by using a minimal manipulation technique in a closed system (Lipogems®), without the addition of enzymes or any additives. The final product will consist of micronized fat tissue yielding fat clusters with preserved vascular stroma of about 500 microns with intact stromal vascular niches and harboring regenerative cellular elements. Approximately 6 mL of micro-fragmented adipose will be injected into the tendon with a 22-gauge needle under continuous ultrasound guidance. No other biological or pharmacological agents will be used in combination with the micro-fragmented adipose. After 24 hours, subjects will be given a standardized stretching protocol to follow for 4 weeks followed by a formal strengthening program. Participants will be followed for adverse events and changes in shoulder pain intensity on an 11-point numerical rating scale (NRS; 0-10, with anchors "no pain" and "pain as bad as you can imagine"); the Wheelchair User's Shoulder Pain Index (WUSPI; 15-item disease-specific functional measure of shoulder pain in persons with SCI); the Brief Pain Inventory interference items (BPI-I7; a subscale of 7 items measuring interference with general activity, sleep, mood, relationships, etc.); and a 5-point subject global impression of change (SGIC) scale. Subjects will be examined at 1 month, 2 months, 3 months, and 6 months after the treatment. Follow-up shoulder ultrasound will be performed at 6 months.
Investigators
Trevor Dyson-Hudson, M.D.
Director, Spinal Cord Injury Research
Kessler Foundation
Eligibility Criteria
Inclusion Criteria
- •The subject is male or female, 18 to 60 years of age, inclusive.
- •The subject has neurological impairment secondary to a spinal cord injury that occurred at least twelve (12) months prior to the Screening Visit and the level of the injury is between C5 and L5, inclusive.
- •The subject is non-ambulatory except for exercise purposes and uses a manual or power wheelchair as his/her primary means of mobility (\> 40 hours/week).
- •The subject currently has chronic shoulder pain due to rotator cuff disease in spite of at least 6 months of conservative treatment (Note: rotator cuff disease will be defined as pain over the anterior shoulder, with direct palpation and pain at the shoulder with provocative tests for rotator cuff disease that is confirmed by tendinopathic changes on ultrasound imaging).
- •The average shoulder pain intensity during the week leading up to the Screening Visit should be at least 4 out of 10 on an 11-point numerical rating scale (NRS; 0, no pain; 10, maximum pain imaginable).
- •The subject is able and willing to comply with the protocol.
- •The subject is able to and has voluntarily given informed consent prior to the performance of any study-specific procedures.
Exclusion Criteria
- •The subject reports prior Lipogems treatment in the same shoulder.
- •The subject reports a history of systemic disorders, such as diabetes or rheumatoid arthritis.
- •The subject has contra-indications to the procedure, such as infection, coagulopathy, or is currently taking anti-coagulants.
- •The subject reports having a glucocorticoid injection in the past 4 weeks.
- •The subject is pregnant (documented by a urine pregnancy test).
- •The subject has any medical condition, including psychiatric disease, which would interfere with the interpretation of the study results or the conduct of the study.
Outcomes
Primary Outcomes
Numerical Rating Scale
Time Frame: Baseline and 4 weeks, 8 weeks, 12 weeks, and 24 weeks after the treatment.
Shoulder pain intensity will also be assessed weekly using a numerical rating scale (NRS). Subjects will be asked to rate their average pain, most severe pain, and least severe pain during the past week using an 11-point scale (i.e. 0-10) anchored at the ends by "no pain" and "pain as bad as you can imagine." An 11-point NRS measure of pain intensity allows for comparison across clinical trials of chronic pain treatment and is recommended as a core outcome measure for chronic pain clinical trials.
Secondary Outcomes
- Brief Pain Inventory interference items (BPI-I7)(Baseline and 4 weeks, 8 weeks, 12 weeks, and 24 weeks after the treatment.)
- Patient Global Impression of Change(Baseline and 4 weeks, 8 weeks, 12 weeks, and 24 weeks after the treatment.)
- Physical Examination of the Shoulder Score (PESS)(Baseline and 4 weeks, 8 weeks, 12 weeks, and 24 weeks after the treatment.)
- Wheelchair User's Shoulder Pain Index (WUSPI)(Baseline and 4 weeks, 8 weeks, 12 weeks, and 24 weeks after the treatment.)