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临床试验/NCT00178425
NCT00178425已完成4 期

Pharmacokinetics of Intravenous / Oral MMF and Oral Tacrolimus in Live Donor and Deceased Donor Liver Transplant Patients

University of Rochester2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2005年1月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
24
试验地点
2
主要终点
Comparison of Pharmacokinetics of MMF in living donor liver transplant and deceased donor liver transplant

研究概览

简要总结

The purpose of this study is to measure the amount of MMF and tacrolimus concentration in the blood at a given time. Currently MMF is ordered as a set dose and tacrolimus is given based on body weight. While the deceased donor transplant receives the complete liver, in the live donor just over half of the liver is given (about 60%). The way these different types of transplants break down drugs could be different. Measuring the drug levels allows us to know what happens to the medication in between the morning and the evening dose.

详细描述

The purpose of this study is to measure the amount of MMF and tacrolimus concentration in the blood at a given time. Currently MMF is ordered as a set dose and tacrolimus is given based on body weight. While the deceased donor transplant receives the complete liver, in the live donor just over half of the liver is given (about 60%). The way these different types of transplants break down drugs could be different. Measuring the drug levels allows us to know what happens to the medication in between the morning and the evening dose.

12 subjects with live liver donors and 12 subjects with deceased donors will be included in the study.

Each patient will have 12 (twelve) blood samples (half a teaspoon) drawn at 0,1, 2, 3, 4, 4½; 5, 6, 7, 8, 10 and 12 hours from an intravenous line placed during the operation. At the same time, 24-hour urine will be collected to measure your kidney function. After 4 to 6 days post transplant when the will be switched to oral MMF, again 10 (ten) blood samples a half teaspoon each will be drawn at 0, 1, 2, 3, 4, 5, 6, 8, 10, 12 hours. Blood will be drawn with the routine daily blood work for the first 14 days and then at 1 and 3 months after transplant. Total blood drawn over 3 months will be about 7 tablespoons. A 24-hour urine will be collected in a container given to you starting one day before the routine clinic visit (as a standard of care). The 24-hour urine will be collected at 1 and 3 months after transplant as well.

If a woman, who could become pregnant, a pregnancy test will be done before your transplant. They would also have to use birth control during the study period and 6 months after the completion of study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
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

入选标准

  • Female patients
  • Negative pregnancy test
  • Willing for contraception during the study period and 6 weeks after study

排除标准

  • Serum Creatinine > 2.5 mg/dl
  • On Dialysis
  • Re-transplantation
  • On Ventilator
  • Multi-organ Transplant
  • Platelets < 50,000
  • WBC < 2,500

结局指标

主要结局

Comparison of Pharmacokinetics of MMF in living donor liver transplant and deceased donor liver transplant

次要结局

  • Comparison of Pharmacokinetics of IV MMF vs PO MMF
  • Pharmacokinetics of tacrolimus after liver transplant

研究者

申办方类型
Other

研究点 (2)

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