Actively Recruiting

Phase Not Applicable
Age: 20Years +
All Genders
ID06913088

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

Age: 20Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Infectious arthritis
  • Acute gout

AI-Screening

AI-Powered Screening

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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 - 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

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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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