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临床试验/NCT00905515
NCT00905515已完成4 期

Optima: Optimizing Prograf Therapy in Maintenance Allografts II

East Carolina University1 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2003年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
63
试验地点
1
主要终点
Optimal Dose of Calcineurin Inhibitor in Long-term Maintenance Kidney Transplant Patients

研究概览

简要总结

This study is designed to optimize calcineurin immunosuppressive regimens and evaluate immunological and non-immunological markers that may explain mechanistic differences in these agents and their effects.

详细描述

One of the major challenges in transplantation over the past two decades has been managing long-term renal function. Serum creatinine is the most commonly used serum marker of renal function. However serum creatinine is insensitive for detecting small decreases in glomerular filtration rate (GFR). Another marker for renal function is cystatin C. Dharnidharka et al concluded that cystatin C is superior to serum creatinine as a marker of kidney function since cystatin C was a more sensitive marker than serum creatinine for detecting decreases in GFR. Pirsch et al reported that tacrolimus-treated patients had a lower incidence of severe acute rejection and better lipid profiles than cyclosporine-treated patients.

Cardiovascular disease is the primary cause of premature death in renal and other transplant recipients. Current immunosuppressive protocols often elevate cardiovascular disease risk factors such as hypertension, hyperlipidemia, obesity and diabetes.

This study is designed to optimize calcineurin immunosuppressive regimens to ensure the best possible long-term outcomes after renal 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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient is the recipient of a cadervic or living donor renal transplant.
  • Patient was 18 years of age at time of transplant.
  • Patient is at least 6 months post-transplant.
  • Patient has been on a cyclosporine-based immunosuppressive regimen since the transplant.
  • Patient has a functioning allograft and a Cockcroft/Gault estimate of creatinine clearance >or= 35 mL/min within four weeks prior to randomization.
  • Patient or legal guardian has signed and dated an Institutional Review Board (IRB) approved informed consent document and is willing and able to follow study procedures.
  • Females are not pregnant and agree to practice effective birth control while receiving immunosuppressant medication.

排除标准

  • Patient is the recipient of a solid organ transplant other than the kidney.
  • Patient experienced biopsy-confirmed, acute rejection, (Banff 97 criteria)within 3 months before randomization that required treatment, which is defined as antilymphocyte therapy, corticosteroids, or an increase in the number or dose of immunosuppressant medication.
  • Patient has recurrence of primary renal disease, or de novo renal disease.
  • Patient has a urine protein of > 1.5g/24 hours or two successive urinalyses sent to and reported by the laboratory indicating albuminuria greater than 2+ within 6 months prior to enrollment.
  • Patient has an estimated creatinine clearance < 35 mL/min calculated using Cockcroft/Gault formula within four weeks prior to randomization.
  • Patient has changed adjunctive immunosuppressant therapy within one month if randomization.
  • Patient is pregnant or lactating.
  • Patient is a known carrier of any of the HIV viruses.
  • Patient has a known or suspected malignancy (except for treated squamous or basal cell skin cancers) < 5 years before randomization or a history of post-transplant lymphoproliferative disease (PTLD).
  • Patient has a known hypersensitivity to tacrolimus, or any of the excipients of the drug.

研究组 & 干预措施

Control Group Cyclosporine

Active Comparator

Maintain on Cyclosporine (CsA) at target trough level of 50-250 ng/mL.

干预措施: cyclosporine (Drug)

Low Trough Level Prograf Group

Active Comparator

Convert to Prograf (TAC) at target trough levels of 3.0-5.9 ng/mL.

干预措施: Prograf (Tacrolimus) (Drug)

High Trough Level Prograf Group

Active Comparator

Convert to TAC at target trough levels of 6.0-8.9 ng/mL.

干预措施: Prograf (Tacrolimus) (Drug)

结局指标

主要结局

Optimal Dose of Calcineurin Inhibitor in Long-term Maintenance Kidney Transplant Patients

时间窗: 3 years

Change in Risk Factors for Cardiovascular Morbidity and Chronic Graft Dysfunction as Evidenced by Blood Levels of Homocysteine

时间窗: 3 years

Renal Function in Patients Converted From Cyclosporine to Prograf

时间窗: 3 years

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paul Bolin

Chair of Internal Medicine

East Carolina University

研究点 (1)

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