ISRCTN13331870进行中（未招募）1 期
An open controlled randomized clinical trial to study the clinical efficacy of the drug Eryxin produced by Namangan Pharm Plant
amangan Pharm Plant LTD0 个研究点目标入组 60 人开始时间: 2024年2月7日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Adults aged 18 years old and over
- •2. Written informed consent to participate in the study
- •3. With rheumatoid arthritis
排除标准
- •1. Pregnancy
- •2. Lactation
- •3. Children aged under 18 years old
- •4. Presence of hypersensitivity to the drug components
- •5. Patient's participation in other clinical trials within the last 30 days
- •6. Absence of informed written consent of the patient to participate in a clinical trial
- •7. Hypersensitivity to the drug
- •8. Genetically determined glucose-6-phosphate dehydrogenase deficiency (risk of hemolytic anemia)
- •9. History of gastrointestinal bleeding or perforation associated with NSAID therapy
- •10. Active peptic ulcer/bleeding or a history of recurrent peptic ulcer/bleeding (two or more cases of confirmed ulcer or bleeding)
- •11. Hypersensitivity reactions (symptoms of asthma, rhinitis, angioedema, or urticaria) to other NSAIDs, including aspirin
- •12. Severe liver dysfunction
- •13. Severe impairment of renal function
- •14. Chronic heart failure in decompensation stage
研究者
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