EUCTR2011-005011-93-GB进行中（未招募）不适用
se of diazoxide in hypoglycaemia - Use of diazoxide in acute hypoglycaemia
niversity of Dundee and NHS Tayside0 个研究点开始时间: 2011年11月18日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •1.Healthy adults (aged 18-55) with >5 years disease duration
- •2.On intensive insulin therapy (CSII or multiple daily injections)
- •3.HbA1C <8.0%
- •4.Ability to give written informed consent to participate in the study
- •5.BMI between 20-29
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 12
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •1.History of significant cardiac, hepatic, renal or neurological disease.
- •2.Significant head injury, epilepsy or hypoglycaemia-induced seizures.
- •3.Pregnancy.
- •4. Participants who are currently breast feeding
- •5.Participants on thiazide diuretics
- •6.Participants on other potassium channel openers (nicorandil, minoxidil)
- •7. Participants already on diazoxide or who have known documented allergy to diazoxide
- •8.Participants on medications with vasodilatory properties such as methyldopa, reserpine, theophyllines and nitrites.
- •9.Participants on hydantoins (fosphenytoin, phenytoin)
- •10.Significant anaemia Hb<11.0 and Hct<33%.
- •11.If they have donated blood in the last 30 days.
- •12.All those who have participated in a CTIMP in the last 3 months
研究者
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