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临床试验/NCT00204191
NCT00204191Unknown4 期

Open, Prospective, Randomized Study to Compare the Efficacy and Safety of Immunosuppression Regimens Based on Cyclosporine (Neoral®) and Tacrolimus (Prograf®) in Renal Transplant Patients

Uniwersytet Mikolaja Kopernika w Toruniu2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2003年5月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
发起方
入组人数
300
试验地点
2
主要终点
patient survival

研究概览

简要总结

The purpose of this study is to evaluate and compare, in the single center setting, the safety, efficacy and cost-effectiveness of the two standard immunosuppressive regimens based on tacrolimus and cyclosporine.

详细描述

Despite several multicenter studies, there is no hard evidence on the superiority of a cyclosporine or tacrolimus based immunosuppressive regimen following kidney transplantation, in a single-center setting. Existing studies concentrated on benefits in safety and efficacy, but seldomly evaluated the cost-effectiveness of one treatment.

The study has been designed in a fashion as close to the daily clinical practice as possible. Patients are randomized in pairs, receiving kidneys from the same donor, thus avoiding donor-related bias. Those having specific indications or contraindications for one of the study medications were not entered into the study. All other study-related decisions are made only on a clinical basis and according to the standard practice of the center. Patients are followed on the intention-to-treat rule. Cost-effectiveness will be calculated on 12-month treatment for each patient entered into the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • First or second cadaveric kidney transplantation
  • Age over 18 years old
  • Specific indications or contraindications for cyclosporine or tacrolimus are absent
  • Informed consent

排除标准

  • Specific indications for use of cyclosporine or tacrolimus
  • Specific contraindications for use of cyclosporine or tacrolimus
  • Participation in another interventional clinical trial
  • Pregnancy or lactation

结局指标

主要结局

patient survival

时间窗: at one year

graft survival

时间窗: at one year

次要结局

  • renal function measured by serum creatinine (SCr)(at one year)
  • lipid profile(throughout the study)
  • total cost of the treatment

研究者

发起方
Uniwersytet Mikolaja Kopernika w Toruniu
申办方类型
Other

研究点 (2)

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