ACTRN12610000428066已完成4 期
A randomised double blind, placebo controlled, cross-over study of the effect of amiloride over 6 weeks, on renal water handling in individuals with a bipolar or unipolar disorder, requiring lithium therapy
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 10
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 60 Years(—)
- 性别
- All
入选标准
- •Inclusion criteria.
- •All patients aged 18 to 60, with a bipolar or unipolar affective disorder requiring the commencement of lithium to manage their psychiatric disorder, and who are able to give informed consent.
排除标准
- •Exclusion criteria.
- •Any individual who is unable to give informed consent.
- •Any patients with evidence of renal impairment (plasma creatinine > 0.12 mmol/l)
- •Any patient unable to comply with a fluid restriction.
- •Any previous exposure to lithium
- •Pregnancy, thyroid disease.
- •Any contraindication to amiloride.
- •Thiazide or Angiotensin converting enzyme inhibitors, requirement for potassium supplements.
研究者
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