EUCTR2020-001084-83-FR进行中（未招募）1 期
rea treatment of hyponatremia during subarachnoid hemorrhage - NAT-URE
CHU Grenoble-Alpes0 个研究点目标入组 52 人开始时间: 2020年4月10日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 52
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
- •Patients at least 18 years old
- •- Non-traumatic subarachnoid hemorrhage
- •- Hyponatremia defined by a serum lower than 135
- •mmol / L and high natriuresis, greater than 250 mmol / L
- •despite well-conducted salt additions
- •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 52
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 52
排除标准
- •- Severe cardiac decompensation (LVEF <30%)
- •- Severe hepatic cirrhosis (PT <30%, ascites), insufficiency
- •known severe renal (GFR <30mL / min / 1.73m²)
- •- Blood urea> 25 mmol / L in the basal state
- •- Osmotherapy and diuretics in the last 48 hours
- •- Ongoing treatment with systemic corticosteroids
- •- All protected persons: woman pregnant, parturient, nursing mother, person deprived of liberty by judicial or administrative decision, person making subject to legal protection.
- •- Patient not affiliated to a social security scheme
- •- Known hypersensitivity to any of the components of energytonyl
- •- Contraindications to energytonyl: taking anticoagulants,
- •diabetic patients treated
研究者
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