Skip to content

The Efficacy of Ultrasonication in Combination With Corticosteroid Intraarticular Injection for Arthritis

The Efficacy of Ultrasonication in Combination With Corticosteroid Intraarticular Injection for Arthritis

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07363876
Enrollment
100
Registered
2026-01-23
Start date
2025-12-29
Completion date
2026-12-31
Last updated
2026-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis, Intra-articular Injections, Rheumatology, Ultrasonication

Brief summary

This study investigates whether ultrasound therapy applied prior to intra-articular corticosteroid injection can enhance the treatment efficacy for patients with joint arthritis and assess its safety. Adult patients diagnosed with arthritis in the limbs who are indicated for corticosteroid injection are eligible, while patients with joint replacement, hip joint involvement, gout, infectious arthritis, or local cellulitis are excluded. Ultrasound therapy is a valuable physical therapy tool for musculoskeletal diseases, producing therapeutic effects through thermal and non-thermal mechanisms. It can improve tissue extensibility, reduce joint stiffness, increase local blood flow, enhance metabolism during tissue repair, and facilitate drug absorption. This study evaluates whether applying ultrasound before intra-articular corticosteroid injection improves therapeutic outcomes in patients with arthritis, and assesses the safety of this combined intervention. Patients aged 18 or older, diagnosed with limb arthritis, and indicated for corticosteroid injection are eligible. Exclusion criteria include joint replacement, hip joint involvement, gout, infectious arthritis, or local cellulitis at the treatment site.

Interventions

DEVICETherapeutic Ultrasound

Therapeutic Ultrasound (TUS) is a non-invasive treatment widely used in physical medicine and rehabilitation for musculoskeletal conditions. Since its introduction in the mid-20th century, TUS has gained popularity in clinical practice due to its ability to penetrate tissues, target treatment areas precisely, and exhibit minimal side effects. This study aims to investigate the mechanisms of action, clinical efficacy, and safety of therapeutic ultrasound in musculoskeletal therapy.

Injection of triamcinolone (3-50 mg depending on joint size) into the affected joint. Administered once per participant.

Sponsors

Taichung Veterans General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 years or older. * Diagnosed with arthritis in the limbs. * Inadequate response to or contraindication for oral anti-inflammatory medications. * Assessed by a physician as requiring intra-articular corticosteroid injection.

Exclusion criteria

* History of joint replacement (prosthetic joint) in the affected area. * Hip joint involvement. * Diagnosis of gout. * Infectious arthritis. * Presence of cellulitis at the treatment site.

Design outcomes

Primary

MeasureTime frameDescription
Reduction in Synovial Swelling Area Assessed by Joint UltrasoundFrom enrollment to the end of treatment at 2 weeksSynovial swelling area (pixels) assessed by joint ultrasound. A treatment response is defined as a ≥50% reduction in synovial swelling area from baseline.
Change in Power Doppler (PD) Score of the Target JointFrom enrollment to the end of treatment at 2 weeksPower Doppler (PD) score (range 0-3) of the target joint assessed by joint ultrasound. A treatment response is defined as a PD score of 0 at 2 weeks post-treatment.
Change in Pain Visual Analogue Scale (VAS)From enrollment to the end of treatment at 2 weeksPain intensity assessed using a visual analogue scale (VAS 0-10). A treatment response is defined as a ≥50% reduction in VAS score from baseline or a VAS score ≤1 at 2 weeks post-treatment.

Secondary

MeasureTime frameDescription
Absence of Synovitis Recurrence Based on Power Doppler (PD) ScoreFrom enrollment to 3 months post-treatmentAbsence of synovitis recurrence assessed by Power Doppler (PD) ultrasound. Recurrence is defined as any increase in PD score compared with the 2-week post-treatment assessment.
Absence of Synovial Swelling Recurrence on Gray-Scale UltrasoundFrom enrollment to 3 months post-treatmentAbsence of synovial swelling recurrence assessed by gray-scale ultrasound. Recurrence is defined as an increase in synovial swelling area of ≥20% compared with the 2-week post-treatment assessment.

Contacts

CONTACTKuo-Lung Lai, MD
kllaichiayi@yahoo.com.tw+886-4-2359-2525
PRINCIPAL_INVESTIGATORKuo-Lung Lai, MD

Taichung Veterans General Hospital (TaichungVGH)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026