跳至主要内容
临床试验/JPRN-UMIN000003245
JPRN-UMIN000003245招募中4 期

A Comparative Study of Neoral in combination with Corticosteroid comparing to Corticosteroid alone in patients with Nephrotic syndrome - A Comparative Study of Neoral in patients with Nephrotic syndrome.

Kyoto university hospital0 个研究点目标入组 50 人开始时间: 2010年2月26日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
50

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
18years-old 至 75years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Exclusion Criteria Patients who meet following criteria will be excluded from this study. 1. Patients with renal impairment that is defined as that creatinin clearance is less than 50ml/min calculated from serum creatinin and from pooled urine creatinin. 2. Patients who are diagnosed as a steroid resistant nephrotic syndrome. 3. Patients who have to take any drugs, which have renal toxicity. 4. Patients with malignancy or history of malignancy. 5. Patients who have uncontrollable hypertension by any treatment. 6. Patients with malabsorption syndrome, cerebral circulatory disturbance or seizure 7. Patients with cardiac, liver or pancreatic severe disease 8. Patients who are pregnancy, lactation or suspicion of pregnancy. 9. Patients who are considered that immunosuppressive drugs should not be used due to infection. 10. Patients who have an episode of allergic reaction to any ingredients of Neoral. 11. Patients who are judged ineligible to enroll into this trial due to any reasons by the study physician.

研究者

相似试验