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临床试验/NCT00275522
NCT00275522已完成4 期

A Randomized Open-label Study to Compare the Safety and Efficacy of Two Different Sirolimus Regimens With a Tacrolimus + Mycophenolate Mofetil Regimen in De Novo Renal Allograft Recipients.

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2005年12月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
Mayo Clinic
入组人数
16
试验地点
1
主要终点
Calculated creatinine clearance at 12 months after transplantation.

研究概览

简要总结

The study is being done to compare the safety and effects (good and bad) of three different combinations of immunosuppression drugs used by kidney transplant recipients while also looking at their kidney function.

详细描述

This is an open-label, randomized, comparative, multinational study. The study will be looking at the kidney function of kidney transplant recipients, while also comparing the safety and the effects (good and bad) of three different combinations of immunosuppression drugs in combination with prednisone, following treatment with Daclizumab (Zenapax). The three combinations are; (1) sirolimus and tacrolimus followed by the withdrawal of tacrolimus after three months; (2) sirolimus and mycophenolate mofetil (MMF); and (3) tacrolimus and MMF. The participants will be required to return to throughout the next 24 months following their transplant for physical exams, chest x-ray, blood, and urine tests. Participants will be put into one of three groups, and receive the study drugs starting on the day of transplant. Due to some drugs affecting the drug levels of sirolimus, participants need to agree not to take any new drugs during the study unless approved by the study doctor.

研究设计

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

入排标准

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

入选标准

  • •Participants must be at least between the ages of 18 and 75, and will be receiving their first or second kidney transplant.

排除标准

  • 未提供

结局指标

主要结局

Calculated creatinine clearance at 12 months after transplantation.

次要结局

  • Calculated creatinine clearance at 26, 78, and 104 weeks post transplantation.
  • Serum creatinine at 26, 52, 78, and 104 weeks post transplantation.
  • Subject and graft survival at 26, 52, 78, and 104 weeks post transplantation.
  • Incidence and severity of biopsy-confirmed acute rejection at 26, 52, 78, and 108 weeks post transplantation.
  • Severity of rejection, including histological grade of the first acute rejection episode.

研究者

发起方
Mayo Clinic
申办方类型
Other

研究点 (1)

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