ISRCTN16794957已完成未知
Determining feasibility of Randomisation to high vs. ad libitum water Intake in Polycystic Kidney Disease: the DRINK randomised feasibility trial
Cambridge University Hospitals NHS Foundation Trust and University of Cambridge0 个研究点目标入组 50 人开始时间: 2016年11月23日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 50
研究概览
简要总结
2018 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/29743334 (added 20/05/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Have given written informed consent to participate
- •2. Aged 16 years or older
- •3. Have a diagnosis of ADPKD (fulfilling radiological diagnostic criteria ± genetic evidence)
- •4. eGFR = 20ml/min/1.73m2
- •5. Able to self-monitor urine SG
排除标准
- •1. Inability to provide informed consent
- •2. eGFR < 20ml/min
- •3. Fluid overload states e.g. heart failure, cirrhosis, or requirement for fluid restriction
- •4. Confounding illness impacting on renal disease e.g. concomitant diabetes or glomerulonephritis
- •5. Treatment with diuretics for fluid overload (those on diuretics for hypertension may participate in the trial after a run-in period of 2 weeks)
- •6. Treatment with Tolvaptan in the last 4 weeks
- •7. Pregnancy or breastfeeding
研究者
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