Individualized Blood Glucose Control in ICU.
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 2,069
- 试验地点
- 12
- 主要终点
- All-cause mortality
研究概览
简要总结
During the last 2 decades, the management of hyperglycemia in critically ill patients has become one of the most discussed topics in the intensive-care field. The initial data suggesting significant benefit from the normalization of blood glucose levels in critically ill patients using intensive intravenous insulin therapy (Van den Berghe G et al. N Engl J Med. 2001) has been tempered by later studies (Finfer S et al. N Engl J Med. 2009). Some studies suggested that strict blood glucose control might benefit in non-diabetic patient and worsen outcomes in diabetics. We hypothesized that an individualized blood glucose target based on glycated hemoglobin measured at ICU admission would improve outcome when compared to a standard care of maintaining blood glucose bellow 10 mmol/l (180 mg/dl). We designed a randomized double blinded study in which Blood glucose control is piloted in both groups by a web-guided protocol that directly gives instruction to nurses (https://extranet.chu-lyon.fr/cpg). The study will enroll 4200 patients in 10 centers. Primary end point is 90 d outcome after randomization.
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
- Double (Participant, Investigator)
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
- •Patients are eligible for INCLUSION in the study if ALL the following criteria are met:
- •Patient is 18 year old or older;
- •At time of the patient's admission to the ICU the treating ICU specialist expects the patient will require treatment in the ICU that extends beyond the calendar day following the day of admission.
排除标准
- •Patients will be EXCLUDED from the study if ONE or MORE of the following criteria are present:
- •Patient or legal surrogate decision maker does not accept the participation to the study;
- •Imminent death (anticipated in less than 48 hours);
- •The treating clinicians are not committed to full supportive care (no resuscitation, no renal replacement therapy limits in dose of vasoactive support);
- •Patient is expected to be eating before the end of the day following admission;
- •Admission in ICU for hypoglycemic encephalopathy or patient at risk for hypoglycaemia ( e.g. known insulin secreting tumour or history of unexplained or recurrent hypoglycaemia or fulminant hepatic failure);
- •If a patient has previously been enrolled in the CONTROLING Study (patients cannot be enrolled in the CONTROLING Study more than once).
研究组 & 干预措施
Individualized blood glucose target
Maintain blood glucose in individualized target based on glycated hemoglobin level (A1c); Blood glucose level is maintained bellow 1.59 × A1c - 1.59 (mmol/l).
干预措施: Human insulin - Insulin administration to control blood glucose level. (Drug)
Conventional blood glucose target
Maintain blood glucose bellow 10 mmol/l.
干预措施: Human insulin - Insulin administration to control blood glucose level. (Drug)
结局指标
主要结局
All-cause mortality
时间窗: 90 days after randomization
次要结局
- incidence and severity of severe hypoglycemia (less than 2.2 mmol/l)(during ICU stay (on average 10 days))
- All-cause mortality(28 days after randomization and at ICU discharge)
- Length of intensive care unit stay(90 days)
- Need for respiratory support, vasopressor support, dialysis and non-prophylactic antibiotics(during ICU stay (on average 10 days))