Last updated: January 2, 2023
Sponsor: Chinese University of Hong Kong
Overall Status: Active - Recruiting
Phase
2
Condition
Arthritis And Arthritic Pain (Pediatric)
Joint Injuries
Musculoskeletal Diseases
Treatment
N/AClinical Study ID
NCT05499312
Gout Study
Ages 18-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patient meeting the American College of Rheumatology (ACR)/European League AgainstRheumatism (EULAR) 2015 gout classification criteria (met sufficient criterion* ortotal score ≥8) ;
- History of >=1 self-reported flare of gouty arthritis within 12 months prior torandomization;
- Agree to undergo blood test and willing to complete questionnaires and takemedications as scheduled; and
- Agree to participate in the study and provide written informed consent. (for thoseilliterate subjects, their family member can sign the consent form upon subject'sagreement) Note: * Sufficient criterion = Presence of MSU crystals in a symptomaticjoint or bursa (i.e., in synovial fluid) or tophus
Exclusion
Exclusion Criteria:
- Liver-kidney yin deficiency pattern according to Chinese medicine theory;
- Use of urate-lowering drugs within 2 weeks prior to screening;
- Present of tophi or known history of kidney stones.
- Known use of oral/injectable corticosteroids or other Chinese herbal medicine fortreating gout within 1 month prior to screening;
- Ongoing acute gout arthritis flare at screening or within 2 weeks prior to screening;
- History of >4 flares overall in the 12 months prior to screening.
- Polyarticular gouty arthritis involving more than 4 joints;
- Severe deformity, stiffness and labor loss of patients with advanced arthritis;
- Known rheumatoid arthritis, evidence/suspicion of infectious/septic arthritis, orother acute inflammatory arthritis;
- Known history of any serious diseases such as severe kidney and liver impairments,autoimmune disease, thyroid disease, Hodgkin's disease, lymphoma, severe mentaldisorders and leukemia
- Known presence or suspicion of acute infectious disease;
- Known history of malignancy within the past 5 years;
- Known allergic to the drug used in this study;
- Documented pregnant or lactation;
- Subjects participating in other clinical studies at the same time.
Study Design
Total Participants: 80
Study Start date:
October 11, 2022
Estimated Completion Date:
February 28, 2025
Study Description
Connect with a study center
The Chinese University of Hong Kong
Sha Tin,
Hong KongActive - Recruiting
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