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临床试验/NCT00478608
NCT00478608已完成3 期

A Clinical Study to Evaluate the Efficacy and Safety of Cyclosporine (CsA) and Sirolimus (SRL) Induction Followed by Cyclosporine Withdrawal in Korean Renal Allograft Recipients

Wyeth is now a wholly owned subsidiary of Pfizer9 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2007年3月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
79
试验地点
9
主要终点
Number of Patients Experiencing Biopsy Confirmed Acute Rejection Through Month 6 After Transplantation.

研究概览

简要总结

Primary : To evaluate the efficacy of sirolimus assessed by the incidence of biopsy-confirmed acute rejection episode at 6 months after transplantation in Korean renal transplantation recipients.

Secondary :

  1. To evaluate the safety of sirolimus over 12 months after transplantation in Korean renal transplantation recipients.
  2. To evaluate graft function, patient survival and graft survival at 6 and 12 months after transplantation, and to investigate the incidence of biopsy-confirmed acute rejection episode at 12 months after transplantation.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Age greater than or equal to 13 years of age.
  • End-stage renal disease in patients scheduled to receive a primary renal allograft from a cadaveric donor, a living-unrelated donor, or from a living-related (excluding 0 antigen mismatch) donor. A mismatch donor is defined as a donor human leukocyte antigen (HLA) antigen not shared by the patient.
  • Patients with a panel of reactive antibody (%PRA) less than or equal to 50%

排除标准

  • Evidence of active systemic or localized major infection at the time of initial sirolimus administration.
  • Evidence of infiltrate, cavitation, or consolidation on chest x-ray obtained during pre-study screening.
  • Chronic anti-arrhythmic therapy for ventricular arrhythmia or other cardiac abnormality contraindicating general anesthesia or surgery.
  • History of malignancy within 5 years before enrollment into the study (with the exception of adequately treated basal cell or squamous cell carcinoma of the skin).
  • Current treatment with partial opioid agonists (eg, buprenorphine) or combination agonists/antagonists.

结局指标

主要结局

Number of Patients Experiencing Biopsy Confirmed Acute Rejection Through Month 6 After Transplantation.

时间窗: 6 months after transplantation

The diagnosis of acute rejection required a kidney biopsy. Biopsies were assessed using the Banff criteria, standardized diagnostic categories based on histological assessments (e.g., cell types and distributions).

次要结局

  • Glomerular Filtration Rate (GFR) (Nankivell Method)(6 and 12 months)
  • Serum Creatinine(Baseline, 6 and 12 months)
  • Patient and Graft Survival(12 months)
  • Number of Patients Experiencing Biopsy Confirmed Acute Rejection Through Month 12 After Transplantation(12 months after transplantation)

研究者

发起方
Wyeth is now a wholly owned subsidiary of Pfizer
申办方类型
Industry

研究点 (9)

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