EUCTR2019-003676-39-NL进行中(未招募)1 期
Effects of sodium lactate infusion in patients with glucose transporter 1 deficiency syndrome (GLUT1DS)
未提供0 个研究点目标入组 4 人开始时间: 2020年6月9日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 4
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
- •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- •- Diagnosed with GLUT1DS and known in our center.
- •- Baseline characteristics include a high frequency of clinical seizures and epileptic discharges on EEG.
- •- History of trying ketogenic diet with good compliance but without beneficial effects.
- •- Age > 6 years.
- •- Informed consent.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 4
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •- Additional medical condition or illness that impairs the patient’s ability to participate in the study (for example actual treatment of a malignancy, active infection, poorly controlled diabetes mellitus, hypertension, organ failure, clinically significant haematological or biochemical abnormalities).
- •- Elevated serum sodium (> 145 mmol/L).
- •- Participation in another interventional study at start of the study or during the study.
- •- Presence of known panic disorders or a history of panic attacks.
研究者
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