EUCTR2018-000756-17-BE进行中（未招募）1 期
Impact of Tight blood Glucose Control within normal fasting ranges with insulin titration prescribed by the Leuven algorithm in adult critically ill patients
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- KU Leuven
- 入组人数
- 9,230
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Adult (=18 years of age) patient admitted to one of the participating intensive care units
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 4300
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 4930
排除标准
- •- Patients with a DNR (do not resuscitate) order at the time of ICU admission
- •- Patients expected to die within 12 hours after ICU admission (= moribund patients)
- •- Patients able to receive oral feeding (not critically ill)
- •- Patients without arterial and without central venous line and without imminent need to place it as part of ICU management (not critically ill)
- •- Patients previously included in the trial (when readmission is within 48 hours post ICU discharge, the trial intervention will be resumed)
- •- Patients already enrolled in another randomized controlled trial (RCT) powered for clinical endpoints
- •- Patients transferred from a non-participating ICU with a pre-admission ICU stay >7 days
- •- Patients planned to receive parenteral nutrition during the first week in ICU
- •- Patients suffering from diabetic ketoacidotic or hyperosmolar coma on ICU admission
- •- Patients with inborn metabolic diseases
- •- Patients with insulinoma
- •- Patients known to be pregnant or lactating
- •- No informed consent
研究者
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