ACTRN12613001021763终止4 期
A double-blind, placebo controlled, crossover study of a nocturnal dose of captopril to determine its effect on diurnal blood pressure and orthostatic symptoms in people with spinal cord injury
Austin Hospital0 个研究点目标入组 4 人开始时间: 2013年9月13日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 发起方
- 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
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Traumatic spinal cord injury
- •Age 18 years or greater
- •Able to provide informed consent
- •Symptoms of orthostatic intolerance
排除标准
- •Known hypersensitivity to captopril or any other ACE inhibitor
- •Significant renal impairment
- •Persistent hyperkalaemia
- •Recent changes or titration of antihypertensive agents or intention to do so within duration of study
- •Presence of any other significant medical conditions likely to influence ability to co-operate or prevent adherence to protocol, or where treatment with captopril would put the participant at increased risk of adverse events or drug interactions
- •Pregnancy or breastfeeding
研究者
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