JPRN-UMIN000010126已完成未知
Efficacy and safety of treatment with moderate doses of corticosteroid and immunosuppressants in rheumatoid arthritis patients with interstitial lung disease - Efficacy and safety of treatment with moderate doses of corticosteroid and immunosuppressants in RA-ILD
Department of Lifetime Clinical Immunology, Tokyo Medical and Dental University0 个研究点目标入组 34 人开始时间: 2013年2月26日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 34
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
- •A patient who has any of the following conditions will be excluded from this study. 1. When a patient has acute exacerbation of interstitial lung disease (when a patient has acutely progressive bilateral lung infiltration and is considered to be inappropriate for the study entry by the attending physician) 2. When a patient has pulmonary hemorrhage 3. When a patient is considered to require positive pressure ventilation (positive pressure ventilation via endotracheal intubation or noninvasive positive pressure ventilation) 4. When a patient is diagnosed as having active respiratory infection or drug-induced pneumonia 5. In a case with ILD of UIP or NSIP pattern, when tacrolimus is contraindicated or a patient has ever treated with tacrolimus for ILD before 6. In a case with ILD of OP pattern, both MTX and tacrolimus are contraindicated or a patient has ever treated by either MTX or tacrolimus for ILD 7. When a patient is considered to require prednisolone with the dose of more than 0.5 mg/kg/day 8. When a patient has moderate or severe pulmonary hypertension or heart failure 9. When a patient has collagen vascular disease other than rheumatoid arthritis (Sjogren's syndrome is permissible) 10. When a patient has severe organ involvement other than interstitial lung disease 11. When a patient is considered as ineligible for this study for any reason by the attending physician
研究者
相似试验
已完成
不适用
Evaluation of the safety and efficacy of low dose transgenic rice containing peptides from Japanese cedar pollen allergens.JPRN-UMIN000016078The Jikei University, School of Medicine21
尚未招募
不适用
Assessment of effectiveness and safety of minimal doses of propofol for sedation for MRI in childreCTRI/2019/11/022044OKMANYA TILAK MUNICIPAL MEDICAL COLLEGE AND LOKMANYA MUNICIPAL GENERAL HOSPITA
招募中
4 期
A clinical trial to study the efficacy and safety of low dose versus standard dose emicizumab prophylaxis in haemophilia A patients.CTRI/2024/01/061593Department of Health Research, India
已完成
1 期
Benefits and harms of using moderately high dose Turmacin, an active ingrediant of turmeric on acute joint pain in healthy volunteersCTRI/2018/03/012367atural Remedies Private Limited15
已完成
不适用
Effect and Safety of dose-escalating treatment of Imidafenacin for Overactive Bladder : CLSS-modified-Self-Assessment Goal Achievement questionnaireOveractive BladderJPRN-UMIN000004894Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan500
