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临床试验/NCT00319189
NCT00319189已完成4 期

Efficacy and Safety of Nateglinide Treatment in Renal Treatment Recipients With Post Transplant Diabetes Mellitus or Impaired Glucose Tolerance

University of Oslo School of Pharmacy2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2002年11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
入组人数
15
试验地点
2
主要终点
Glucose tolerance

研究概览

简要总结

The objective of the present study is to evaluate both the efficacy and safet of nateglinide in renal transplanta recipients with posttransplant diabetes mellitus or impaired glucose tolerance. Primarily will the change in glucose tolerance and acute insuline responce be addressed.

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
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

  • Reduced glucose tolerance (fasting glucose < 6.1 mmol/L AND 2 hour glucose between 6.7 and 9.9 mmol/L) or posttransplant diabetes mellitus (fasting glucose > 6.1 mmol/L OR 2 hour glucose between >= 10.0 mmol/L)
  • Stable patients fgollowing renal transplantation, less than 25% variation in serum creatinine last week and serum creatinine < 200 micromol/L

排除标准

  • Patients with indulin dependent diabetes mellitus before or after transplantation
  • Planned change in daily prednisolone dose during the study period
  • Haemoglobin < 8g/dL

结局指标

主要结局

Glucose tolerance

Insuline release

次要结局

  • Glucose oxidation
  • Postprandial hyperlipidemia
  • Glomerular filtration rate
  • HbA1C
  • Fasting glucose
  • Plasma nitric oxide
  • Plasma endothelin-1

研究者

发起方
University of Oslo School of Pharmacy
申办方类型
Other

研究点 (2)

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