Actively Recruiting
Clinical Study of Myofascial Trigger Points Injection for Chronic Musculoskeletal Pain and Shoulder Osteoarthritis
Led by Beijing Tiantan Hospital · Updated on 2026-01-16
1036
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating treatments for chronic musculoskeletal pain, specifically shoulder osteoarthritis, a common condition among older adults in China that significantly affects quality of life. This study compares the long-term effects of glucocorticoid injections at myofascial trigger points (MTrPs) versus injections directly into the shoulder joint. The purpose is to see if MTrPs injections are as effective as intra-articular injections, potentially offering an easier and safe treatment option for patients who have not responded to other therapies. Participants will be randomly assigned to receive either an intra-articular shoulder injection or an MTrPs injection. The intra-articular injection includes a combination of lidocaine and triamcinolone acetonide delivered via an anterolateral approach. The MTrPs injection involves injecting a mixture of triamcinolone acetonide, lidocaine, and saline into tender points using a small needle. Injections are given as a single bolus into each trigger point. After treatment, participants will be followed for two years to monitor their pain and function. During the study, participants will have their pain levels assessed at multiple time points using the Numerical Rating Scale (NRS), WOMAC scores, and the Patient Global Impression of Change (PGIC) scale at 2, 4, 8, 12, and 24 weeks. Adverse reactions will be recorded throughout the study, which lasts about one year on average for safety monitoring. The primary outcome is the NRS pain score at 4 weeks. This detailed follow-up will help determine the long-term benefits and safety of both injection methods.
CONDITIONS
Brief Title
Clinical Study of Myofascial Trigger Points(MTrPs) Injection in the Treatment of Shoulder Osteoarthritis(OA)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of shoulder osteoarthritis confirmed by X-ray (Kellgren-Lawrence grade 1-4) and physical exam with at least one myofascial trigger point
- Disease duration longer than 3 months
- Age 45 years or older
- Pain score of 3 or higher on the Numerical Rating Scale despite prior conservative treatment
- Signed informed consent form
You will not qualify if you...
- Allergy history to corticosteroids or trial medications
- Alcohol abuse or long-term opioid use exceeding 2 weeks or more than 3 days per week for over 1 month
- Use of sedative or analgesic medications or long-term steroid therapy
- Severe neurological disorders, liver or kidney dysfunction, heart failure, coagulation issues, gastric ulcer, diabetes, or inflammatory rheumatic diseases
- Intra-articular injection in the past 6 months or planned joint replacement surgery
- Inability to use pain assessment scales
- Presence of local or systemic infection
- Pregnant or breastfeeding women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 24 weeks
Participants receive injections either into the joint cavity or at myofascial trigger points to treat shoulder osteoarthritis.
Visits at 2, 4, 8, 12, and 24 weeks for treatment assessments
Duration - Up to 1 year
Participants are monitored for adverse reactions and overall outcomes after treatment completion.
Regular follow-up visits through study completion
Trial Site Locations
Total: 1 location
1
Beijing Tiantan Hospital
Beijing, Beijing Municipality, China, 100070
Actively Recruiting
Research Team
F
Fang Luo
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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