Actively Recruiting
Clinical Study of Myofascial Trigger Points Injection Compared to Joint Cavity Injection for Treating Hip 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, focusing on hip osteoarthritis, which is common and significantly affects quality of life, especially in older adults. This study compares two types of glucocorticoid injections: one at myofascial trigger points and another directly into the joint cavity. The goal is to see if the easier trigger point injection is as effective as the joint injection over the long term. Participants are randomly assigned to receive either a joint cavity injection or a myofascial trigger points injection, both using triamcinolone acetonide combined with lidocaine. The joint injection is given via an anterolateral approach with a specific mixture of lidocaine and corticosteroid, while the trigger point injection involves injecting each tender point with a small volume of solution using a fine needle. Treatments are followed by regular assessments. Participants will be monitored and evaluated at 2, 4, 8, 12, and 24 weeks after treatment, with follow-up lasting up to 2 years. Researchers will record pain scores using the Numeric Rating Scale (NRS), assess joint function with WOMAC scores, gather patient impressions of change with the PGIC scale, and track any adverse reactions. This detailed follow-up aims to determine the long-term safety and effectiveness of both injection methods.
CONDITIONS
Brief Title
Clinical Study of Myofascial Trigger Points(MTrPs) Injection in the Treatment of Hip Osteoarthritis(OA)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of hip osteoarthritis confirmed by at least two doctors with radiographic evidence
- Physical exam confirming at least one myofascial trigger point
- Disease duration longer than 3 months
- Age 45 years or older
- NRS pain score of 3 or higher despite prior conservative treatment
- Signed informed consent form
You will not qualify if you...
- Allergy to corticosteroids or trial medications
- Alcohol abuse or long-term opioid use exceeding 2 weeks or over 3 days per week for more than 1 month
- Use of sedative or analgesic medications or long-term steroid therapy
- Severe neurological disorders, liver or kidney dysfunction, heart failure, coagulation problems, gastric ulcers, diabetes, or inflammatory rheumatic diseases
- Intra-articular injection within past 6 months or planned joint replacement surgery
- Unable 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.
1 visit (in-person)
Duration - Single injection visit
Participants receive either a myofascial trigger points (MTrPs) injection or a joint cavity injection with triamcinolone acetonide to treat hip osteoarthritis.
1 visit (in-person)
Duration - Up to 24 weeks with safety monitoring up to 1 year
Participants are monitored for pain scores, joint function, patient impressions of change, and adverse reactions following the injection treatment.
Visits at weeks 2, 4, 8, 12, and 24; additional safety monitoring 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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