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临床试验/NCT01663805
NCT01663805Unknown4 期

Effects of the Use of "de Novo" Everolimus for the Expression of Cytokines in Kidneys From Extended Criteria Donors and With Delayed Graft Function

MARIO ABBUD FILHO1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
80
试验地点
1
主要终点
Molecular profile of cytokines

研究概览

简要总结

This is an open, randomized, single-center study. The selected patients will be first divided into two major groups according to the type of organ to be transplanted: standard criteria donor (SCD) or extended criteria (ECD) kidney. Then, each group will be randomly allocated to one of the treatments: tacrolimus (TAC) or everolimus (EVL).

All patients received induction therapy with basiliximab (BXB) and maintenance with Mycophenolate Sodium (MYF) and prednisone (P). This study will evaluate as Primary objectives: To characterize the molecular profile of cytokines in kidneys obtained from deceased donors such as "standard" (SCD) and extended criteria (ECD) in biopsies taken before and after transplantation and to evaluate the effect of treatment with everolimus (EVL) in the expression of these molecules. And as Secondaries objectives: To correlate the pattern of cytokines with delayed graft function (DGF), cold ischemia time, episodes of acute rejection and patient and graft survival.

详细描述

A total of 80 patients will participate in the study, being distributed into 4 groups of 20 individuals. In a pilot study to assess the interventional effect of the mmediate use of EVL on the cytokine profile of ECD and SCD kidneys, compared to conventional immunosuppressive therapy with TAC, no statistical power analysis could be performed a priori.

Definitions of Extended Criteria Donor and Delayed Graft Function (DGF) Deceased donors aged ≥ 60 years or aged between 50 and 59 years and with at least two of the following risk factors: history of systemic hypertension terminal creatinine levels > 1.5 mg/dL or death by a cerebrovascular accident.

DGF (delayed graft function) is defined as the need for dialysis in the first 7 days after transplantation.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years (black and white subjects);
  • End-stage renal disease with indication for transplantation (primary deceased-donor kidney transplant)
  • "Standard" traditional (SCD) or extended criteria (ECD) donor;
  • Informed consent form duly signed before SCD or ECD kidney transplantation.
  • Exclusion criteria:
  • The subject, in the opinion of the investigator, is not able to complete the study protocol;
  • Recipient of live-donor kidney graft;
  • Multiple organ transplant recipient;
  • Evidence of large systemic or localized infection;
  • Evidence of infiltration, cavitation or consolidation on chest X-rays obtained during the evaluation in the screening / baseline visit;
  • Use of any drug under investigation or treatment until up to 4 weeks before transplantation;
  • Known or suspected hypersensitivity to tacrolimus, everolimus or mycophenolate sodium;
  • Immunosuppressive therapies in addition to those described for this study;
  • Hypersensitized patients (PRA > 30%);
  • Patients with HIV+ or Hepatitis B or C virus infection.
  • Patients for whom T0 and T15 biopsies were not taken.

排除标准

  • 未提供

研究组 & 干预措施

Everolimus

Active Comparator

SCD/ECD: BXB (2x20mg, D1 and D4) + EVL (3.0 -8.0ng/ml) + MYF (1440mg/d)+ Prednisone

干预措施: Everolimus (Drug)

结局指标

主要结局

Molecular profile of cytokines

时间窗: 12 months

To characterize the molecular profile of cytokines in kidneys obtained from deceased donors such as "standard" (SCD) and extended criteria (ECD) in biopsies taken before and after transplantation and to evaluate the effect of treatment with everolimus (EVL) in the expression of these molecules.

次要结局

  • Pattern of cytokines with DGF, cold ischemia time, episodes of acute rejection(12 months)

研究者

发起方
MARIO ABBUD FILHO
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

MARIO ABBUD FILHO

Principal Investigator

Instituto de Urologia e Nefrologia

研究点 (1)

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