Autosomal Dominant Polycystic Kidney Disease Data Repository
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 1,000
- 试验地点
- 1
- 主要终点
- Polycystic kidney disdease data repository
研究概览
简要总结
Autosomal dominant polycystic kidney disease (PKD) is the most common inherited kidney disease, affecting more than 400,000 people in the U.S. and 5 million people worldwide. PKD is the 4th most common cause of kidney failure requiring dialysis and/or transplantation. Over half of all PKD patients develop kidney failure by age 60 years, although age of onset of kidney disease varies widely, even among members of the same family.
Despite the fact this is a relatively common problem, relatively few patients have been studied for a sufficient period of time to fully understand how patients are affected over the course of their lifetime. The reason for creating this repository is to collect information about PKD so that the investigators may fully understand its complications, including high blood pressure, heart attack, and stroke. This information may also aid in the development of improved treatment strategies.
详细描述
Visit #1:
- An initial detailed history, physical examination, and laboratory evaluation
- An extensive family history of PKD will be obtained from the patient.
Follow-up Study Visits:
- Patients will return to the outpatient facility for detailed follow-up examinations every other year after Visit 1.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Any person, age 18 or older, with previously diagnosed ADPKD is eligible to participate.
排除标准
- •Inability to provide informed consent.
结局指标
主要结局
Polycystic kidney disdease data repository
时间窗: 30 years
Polycystic kidney disease data repository
次要结局
未报告次要终点
