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临床试验/NCT00830297
NCT00830297已完成2 期

Treat-to-target Trial of Basal Insulin in Post-transplant Hyperglycemia (TIP): Efficacy and Safety of a Novel Protocol in Renal Transplant Recipients Receiving a Tacrolimus-based Immunosuppression

Marcus Saemann1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2009年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
The primary endpoint is the difference in HbA1c between the two study arms.

研究概览

简要总结

Treat-to-target trial of basal Insulin in Post-transplant hyperglycemia (TIP): efficacy and safety of a novel protocol in renal transplant recipients receiving a tacrolimus-based immunosuppression

DESCRIPTION:

A prospective, randomized safety and efficacy study of long-acting insulin (Insulatard®) as therapy against post-transplant hyperglycemia in renal transplant recipients

OBJECTIVES:

Primary Objective:

To demonstrate superiority of long-acting insulin (Insulatard®) against post-transplant hyperglycemia, in comparison to conventional treatment, and as evaluated by HbA1c

Secondary Objectives:

  • To assess the average post-transplant glucose levels in renal transplant patients under conventional blood-glucose lowering therapy during a period of at least 14 days after transplantation by measuring the capillary blood glucose levels four times daily in both groups of patients (fasting, before lunch, before supper, after supper)
  • To detect the number of post-transplant patients who - without any history of pre-transplant diabetes - develop at least one episode of post-transplant hyperglycemia (> 140 mg/dl before supper)
  • To detect the average number of hyperglycemic episodes in post-transplant patients with at least one episode of post-transplant hyperglycemia and without any history of diabetes
  • To assess the amount of (long-acting) insulin (in IU) needed in order to obtain a target capillary blood glucose level in the range of 110 mg/dl to 120 mg/dl before supper in post-transplant patients with incidence of hyperglycemia
  • To assess the safety of long-acting insulin in controlling post-transplant hyperglycemia (especially with regards to episodes of hypoglycemia (glucose-level < 60 mg/dl)
  • To assess the prevalence of post-transplant diabetes, as diagnosed by an abnormal oral glucose tolerance on days 90, 180 and 360 after transplantation, in the group of patients which has been treated with long-acting insulin, in comparison to patients who received conventional treatment
  • To assess the morbidity (hospitalization, infections, subsequent episodes of surgery, requirement of non-immunosuppressive, non- blood glucose lowering medication) in the group of patients with long-acting insulin for hyperglycemia, in comparison to patients randomized into the group receiving conventional treatment
  • To assess the renal outcome (creatinine levels, rejections) in the group of patients which is foreseen to be treated with long-acting insulin for hyperglycemia, in comparison to patients randomized into the group receiving conventional treatment

详细描述

DESIGN / PHASE:

Prospective, single-center, randomized, parallel group, controlled, phase II study.

STUDY PLANNED DURATION:

First patient First visit 1Q 2009 Last patient First visit 4Q 2009 Last patient Last visit 4Q 2010

CENTERS:

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • renal transplantation (deceased or living donor)
  • eligibility for the standard immunosuppression of our center, consisting of tacrolimus, mycophenolate mofetil or mycophenolic acid, dexamethasone/prednisone triple therapy
  • informed consent of the patient

排除标准

  • patients with type 1 or type 2 diabetes
  • allergy against long-acting insulin

研究组 & 干预措施

1 Insulatard (long-acting insulin)

Active Comparator

干预措施: Insulatard (long-acting insulin) (Drug)

2 Conventional treatment

Active Comparator

干预措施: Conventional (Drug)

结局指标

主要结局

The primary endpoint is the difference in HbA1c between the two study arms.

时间窗: post-transplant day 90

次要结局

  • Capillary blood glucose profiles in each group(post-transplant day 1-21)
  • Number of patients and overall number of days with hyperglycemia >140 mg/dl before supper (in each group)(post-transplant day 1 - 21)
  • Number of patients and overall number of days with hyperglycemia >200 mg/dl (in each group)(post-transplant day 1-21)
  • Number of patients and overall number of days with hypoglycemia <60 mg/dl in each group(post-transplant day 1-21)
  • Number of patients with abnormal glucose tolerance(post-transplant day 90, 180 and 360)
  • Difference in HbA1c between the two study arms(post-transplant day 180 and 360)

研究者

发起方
Marcus Saemann
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Marcus Saemann

Ass. Prof. Dr. Marcus Säemann

Medical University of Vienna

研究点 (1)

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