JPRN-UMIN000016048尚未招募未知
Evaluation of intravenous regional block with low- dose infliximab for patients with Complex Regional Pain Syndrome - Evaluation of intravenous regional block with low- dose IFX for patients with CRPS
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 5
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
- 年龄范围
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1. The following laboratory data Hb<8.5g/microliter WBC<3.5*1000cells/microliter Neutrophil<1.0*1000cells/microliter PLT<5*10000cells/microliter ALT or AST>1.5*ULN Total Bilirubin>ULN Cr>=2.0mg/dL (NT-pro BNP>=125pg/ml) 2. Patients have severe, progressive or uncontrolled kidney disease, liver disease, skin disease, blood disease, digestive disease, endocrine disease, lung disease, cardiac disease, or neurological disease. 3. Patients had been hospitalized within 3 months for cardiac event(myocardial infarction or unstable angina), stroke or TIA. 4. Patients had severe infection within 2 months. 5. Patients have congestive heart failure in NYHA class 2 to 4. 6. Patients had relapse or progressive infectious disease including chronic renal infection, chronic chest infectious disease or urinary tract infection. Patients have past history of open drainage wound or ulcer. 7. Abnormal finding of interstitial pneumonia, tuberculosis, or other diseases on chest X-ray within 3 months 8. Past history of demyelinating disease including multiple sclerosis or optic neuritis 9. Patients have past history of gastrointestinal perforation or have active diverticulitis. 10. Patients had non-tuberculous mycobacterial infection or opportunistic infection within 6 months. 11. Hepatitis C positive 12. Hepatitis B positive 13. Patients have malignant neoplasm or had it within 5 years 14. Pregnant or lactating mother 15. Patients have steroid medication. 16. Investigator considers that the enrollment in this study is not benefit for the patient or intravenous regional sympathetic nerve blocking is impossible for the patient.
研究者
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