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The Benefits of Intensive Glycemic Control in Elderly Patients With Type 2 Diabetes

2010年7月23日 更新者:Taipei Veterans General Hospital, Taiwan

Aims/hypothesis:

Populations worldwide are aging and type 2 diabetes is common in individuals aged >80 years. The important issue that needs to be considered is whether tight glycemic control is benefits for elderly patients with type 2 diabetes. The benefits of intensive glucose control remain uncertain for the heterogeneous population of older diabetic patients due to a lack of clinical trial data evaluating the benefits of long-term intensive glucose control in older patients. This study is designed to provide reliable evidence on the balance of benefits and risks conferred by intensive glucose control in elderly patients with type 2 diabetes Methods: This is a prospective, randomized, open-labeled, controlled design to assess the benefits of treating elderly patients with type 2 diabetes. The study will include 208 elderly patients with type 2 diabetes and follow-up for 5 years. Eligible patients are randomized to receive intensive (A1C <7.0%) or conservative (A1C around 8.0%) glycemic control. The primary study outcomes are a composite of macrovascular events and a composite of microvascular events, considered both jointly and separately. The secondary outcomes are death from any cause, death from cardiovascular causes, total coronary events, total cerebrovascular events, heart failure, peripheral vascular events, all cardiovascular events, and hospitalization for 24 hours or more.

Expected results: This study is designed to provide reliable evidence on the balance of benefits and risks conferred by intensive and conservative glucose control in elderly patients with type 2 diabetes. Once completed, this trial will clearly influence the management of elderly patients with type 2 diabetes, regardless of the results.

研究概览

研究类型

介入性

注册 (预期的)

208

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Taipei、台湾、11217
        • 招聘中
        • Chen-Hsen Lee
        • 接触:
          • Harn-Shen Chen, MD, PhD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

80年 及以上 (年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Men or women aged ≥80 years at time of randomization.There is no upper age limit.
  • Be able to walk by themselves
  • They had their first diagnosis of type 2 diabetes mellitus at age 30 years or older.

Exclusion Criteria:

  • Known advanced diabetic complications (such as proliferative retinopathy, chronic kidney disease stage IV or above).
  • Overt clinical congestive heart failure (CHF) requiring treatment with a diuretic or ACE inhibitor.
  • Previous documented cerebral or subarachnoid haemorrhage in the last 6 months
  • Condition expected to severely limit survival
  • Clinical diagnosis of dementia
  • Resident in a nursing home

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:1
Fasting plasma glucose (mg/dL) 90 to 130 Glycated hemoglobin (%) 6.0 to 7.0
Intensive glycemic control
有源比较器:2
Fasting plasma glucose (mg/dL) 90 to 180 Glycated hemoglobin (%) 7.0 to 9.0
OADs and insulin

研究衡量的是什么?

主要结果指标

结果测量
大体时间
The primary study outcomes are a composite of macrovascular events and a composite of microvascular events, considered both jointly and separately.
大体时间:Every 6 months and up to 5 years
Every 6 months and up to 5 years

次要结果测量

结果测量
大体时间
The secondary outcomes are death from any cause, disability from any cause, total coronary events, total cerebrovascular events, heart failure, peripheral vascular events, all cardiovascular events, and hospitalization for 24 hours or more.
大体时间:Every 6 months and upto 5 years
Every 6 months and upto 5 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2009年2月1日

初级完成 (预期的)

2014年12月1日

研究完成 (预期的)

2020年12月1日

研究注册日期

首次提交

2009年2月23日

首先提交符合 QC 标准的

2009年2月24日

首次发布 (估计)

2009年2月25日

研究记录更新

最后更新发布 (估计)

2010年7月26日

上次提交的符合 QC 标准的更新

2010年7月23日

最后验证

2010年6月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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