KCT0005580招募中未知
Genetic identification of hereditary cystic kidney diseases for implementing precision medicine
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 1,200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- o Limit 至 o Limit（—）
- 性别
- All
入选标准
- •Patients with 3 or more cysts in kidneys
- •-Typical ADPKD
- •-Atypical ADPKD
- •-Tuberous sclerosis complex
- •-von Hippel-Lindau disease
- •-Autosomal dominant tubulo-interstitial kidney disease
- •-Autosomal recessive polycystic kidney disease
- •-Nephronophthisis
排除标准
- •Those who are not able to give informed consent or pregnant will be excluded from enrollment. The cases of simple renal cyst and acquired cystic kidney disease which involve cyst formation as the result of renal failure will also be excluded from this study.
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