Actively Recruiting

Phase Not Applicable
Age: 45Years +
All Genders
ID07347028

Clinical Study of Myofascial Trigger Points Injection and Intra-Articular Injection for Knee Osteoarthritis and Chronic Musculoskeletal Pain

Led by Beijing Tiantan Hospital · Updated on 2026-01-16

1036

Participants Needed

1

Research Sites

26 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are studying chronic musculoskeletal pain (CMP), focusing on knee osteoarthritis, a common type of CMP that significantly affects quality of life, especially among older adults. This study compares the long-term effects of glucocorticoid injections at myofascial trigger points (MTrPs) with complex intra-articular injections in treating knee osteoarthritis. It is a prospective, randomized, controlled, and blinded trial designed to evaluate the clinical efficacy between these two injection methods. Participants will be randomly assigned to one of two groups: one receiving glucocorticoid injections at MTrPs and the other receiving intra-articular injections in the knee joint cavity. MTrPs injections use a combination of triamcinolone acetonide, lidocaine, and saline, administered directly into trigger points with a 25-gauge needle. The joint cavity injection group receives an intra-articular knee injection with a similar solution. The treatment aims to assess if the simpler MTrPs injection is not less effective than the intra-articular approach. During the study, patients will be followed for two years with assessments at 2, 4, 8, 12, and 24 weeks after treatment. Researchers will record pain intensity using the Numerical Rating Scale (NRS), functional status with the WOMAC score, patient-reported changes via the Patient Global Impression of Change (PGIC) scale, and any adverse reactions. These evaluations will help understand the treatments' safety and impact over time, supporting better clinical management for knee osteoarthritis.

CONDITIONS

Brief Title

Clinical Study of Myofascial Trigger Points(MTrPs) Injection in the Treatment of Knee Osteoarthritis(OA)

Who Can Participate

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of knee osteoarthritis confirmed by X-ray (Kellgren-Lawrence grade 1-4) by at least two specialists
  • Presence of at least one myofascial trigger point on physical examination
  • Disease duration longer than 3 months
  • Age 45 years or older
  • Pain score of 3 or higher on the Numerical Rating Scale despite previous conservative treatment
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Allergy to corticosteroid medications used in the trial
  • History of alcohol abuse or long-term opioid use
  • Use of sedative or analgesic medications or long-term steroid therapy
  • Severe neurological, liver, kidney, heart, coagulation, gastric, diabetic, or inflammatory rheumatic diseases
  • Intra-articular injection within the past 6 months or planned knee replacement surgery
  • Inability to use pain assessment scales
  • Presence of local or systemic infection
  • Pregnancy or breastfeeding

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.

1 visit (in-person)

Treatment

Duration - Single treatment with follow-up assessments up to 24 weeks

Participants receive either MTrPs injection or intra-articular knee injection with triamcinolone acetonide for knee osteoarthritis.

Visits at Weeks 2, 4, 8, 12, and 24

Follow-up

Duration - Up to 1 year

Participants are monitored for adverse reactions and assessed for pain and function after treatment.

Periodic visits as scheduled 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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