Efficacy and Safety of Simiaowan in Prevention of Acute Flares in Chronic Gout Patients Initiatin… (NCT04069325) | Clinical Trial Compass
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Efficacy and Safety of Simiaowan in Prevention of Acute Flares in Chronic Gout Patients Initiating Febuxostat Therapy
China72 participantsStarted 2019-09-01
Plain-language summary
The aim of this study is to evaluate the efficacy and safety of simiaowan in prevention of acute flares in chronic gout patients initiating febuxostat therapy.
Who can participate
Age range18 Years – 75 Years
SexALL
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Inclusion Criteria:
* Male or female subjects aged 18 to 75 years (time of get informed consent)
* Meet the American College of Rheumatology/The European League Against Rheumatism criteria (2015) for the classification of acute arthritis of primary gout
* Pain Visual Analogue Scale Score (VAS) ≤ 3 at screening
* Serum uric acid ≥7 mg/dL (420μmol/L) at screening
* Self-reported history of at least 2 gout flares within 12 months prior to screening
* Normal electrocardiogram (ECG), or no clinical significant at screening
* Be capable of understanding and complying with protocol requirements
Exclusion Criteria:
* Occurrence of an acute gout flare ongoing at screening or within 2 weeks prior to screening
* Known or suspected of secondary hyperuricemia (e.g. due to renal disorder, hematological disorder, drugs, radiotherapy, chemotherapy or organ transplant)
* Use of colchicine, allopurinol, probenecid, benzbromarone, febuxostat or history of intra-articular steroid injection within 4 weeks prior to screening
* Use of glucocorticoids, nonsteroidal antiinflammatory drugs (NSAIDs), or cyclooxygenase-2 (COX-2) inhibitors within 1 week prior to screening
* History of stroke, transient ischemic attack (TIA), acute myocardial infarction (MI), heart failure (NYHA Class II-IV), coronary intervention procedure (including but not limited to angioplasty, stent placement, coronary revascularization) prior to screening
* History of gastrointestinal (GI) bleeding, peptic ulcer disease prior t…
What they're measuring
1
Proportion of subjects experiencing ≥ 1 gout flare within 12 weeks
Timeframe: Day 1 to Week 12
Trial details
NCT IDNCT04069325
SponsorGuang'anmen Hospital of China Academy of Chinese Medical Sciences