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
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
- 否
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)
干预措施: Insulatard (long-acting insulin) (Drug)
2 Conventional treatment
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
Marcus Saemann
Ass. Prof. Dr. Marcus Säemann
Medical University of Vienna
