Actively Recruiting

Phase Not Applicable
Age: 45Years +
All Genders
ID07347054

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

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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

Follow-up

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

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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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