Actively Recruiting
Ultrasonication-mediated Microbubbles Dressings Increase the Therapeutic Efficacy of Piroxicam Gel for Hand Arthritis: Assessments Using Conventional and Ultrafast Power Doppler Imaging
Led by National Taiwan University · Updated on 2025-04-17
60
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effect of an ultrasonication-mediated microbubbles dressing combined with piroxicam gel for treating hand arthritis in adults. The study aims to find out if adding this dressing improves treatment effectiveness and to assess its safety. Participants with hand arthritis will be compared across three groups to see which approach works best. The trial has three groups: one uses the microbubbles dressing with piroxicam gel, applied on specific days; the second uses ultrasonication with pure gel plus piroxicam gel; and the third uses piroxicam gel alone for one week. Ultrasonication treatments occur on days 1, 3, and 5, while piroxicam gel is applied on days 2, 4, 6, and 7 or daily for the gel-only group. Participants will visit the clinic on day 1 and day 8 for checkups and tests. They will keep a symptom diary throughout the week. Researchers will measure clinical responses and imaging responses using B-mode and power Doppler on day 8 to evaluate treatment effects and safety. The study is randomized with single masking and led by National Taiwan University.
CONDITIONS
Brief Title
Ultrasonication-mediated Microbubbles Dressing for Hand Arthritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of hand arthritis
- At least three symptomatic joints over wrist, metacarpophalangeal joints, and interphalangeal joints
- Age 20 years or older
You will not qualify if you...
- Infectious arthritis
- Acute gout
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 - 7 days
Participants receive ultrasonication treatment on days 1, 3, and 5 along with piroxicam gel application during days 1 to 7 depending on group assignment.
7 visits including ultrasonication on days 1, 3, 5 and gel application on days 1 to 7
Trial Site Locations
Total: 1 location
1
Taichung Veterans General Hospital
Taichung, Taichung, Taiwan, 407
Actively Recruiting
Research Team
K
Kuo-Lung Lai
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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