NCT06601829招募中不适用
Congenital Hepatic Fibrosis and Autosomal Recessive Polycystic Kidney Disease in Children at Sohag University Hospital
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- incidence of congenital hepatic fibrosis in patient with autosomal recessive polycyctic kidney disease
研究概览
简要总结
polycystic kidney disease is aherditary disorder characterized by the formation of numerous fluid filled cysts in the kidneys which can lead to progressive renal impairment PKDencompasses aspectrum of disorders with autosomal dominant polycystic kidneydisease and autosomal recessive polycystic kidney disease being the two main types
研究设计
- 研究类型
- Observational
- 观察模型
- Case Crossover
- 时间视角
- Cross Sectional
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •pediatric patients aged 0-18 years both male and female patients
排除标准
- •patients whose guardians dont provide informed consent patients who are not complient with follow up vists and data collection protocols
结局指标
主要结局
incidence of congenital hepatic fibrosis in patient with autosomal recessive polycyctic kidney disease
时间窗: 12 months
describe congenital hepatic fibrosis in patient with autosomal recessive polycystic kidney explaining their clinical manifestations.diagnosis.managment and complications
次要结局
未报告次要终点
研究者
Sherein Awad Mohamed
Resident-pediatric department-sohag hospital university
Sohag University
研究点 (1)
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