JPRN-UMIN000021267已完成未知
ongitudinal Efficacy and Safety Study of Tolvaptan on Autosomal Dominant Polycystic Kidney Disease Patients - Efficacy Study of Tolvaptan on ADPKD Patients [LET-PKD study]
Autosomal Dominant Polycystic Kidney Disease Research Section, Kyorin University, School of Medicine0 个研究点目标入组 119 人开始时间: 2016年3月12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
- 119
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1) Patients who have been taking tolvaptan since the TEMPO study 2) Patients who are not eligible, at the discretion of Kyorin University Hospital, to take tolvaptan for the stated indication according to the criteria for careful administration of Samsca as specified by the Ministry of Health, Labour and Welfare - Patients with a history of hypersensitivity to tolvaptan or similar chemical compounds - Patients who do not feel thirsty or have difficulty swallowing water - Patients with hypernatremia - Patients with eGFR less than 15 mL/min/1.73 m2 - Patients with chronic hepatitis, drug-induced hepatic dysfunction or other hepatic dysfunctions - Pregnant women or women suspected of being pregnant. Female patients who wish to become pregnant
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