Institutional Registry of Liver Transplantation
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 500
- 试验地点
- 1
- 主要终点
- Time to mortality
研究概览
简要总结
The Institutional Registry of Liver Transplantation is a system for data collection related to patients with liver disease who are possible candidates for liver transplantion. This tool was designed by a multidisciplinary team that includes hepatologists, surgeons, informatics and biostatisticians. It intends to collect the information from the clinical evaluation, physical examination, complementary diagnostic methods and laboratory data. The information is captured sistematically, following structured, standardized and monitored processess to ensure the quality of the data obtained.
The aim is to use the available technology to generate a complete database that can be used to answer research questions.
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 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with indication for liver transplantation
- •Patients who are followed by the Liver Transplantation Unit of Hospital El Cruce
排除标准
- •Patients who deny to participate after the informed consent process.
结局指标
主要结局
Time to mortality
时间窗: 5 years
All patients are followed from the date of the inclusion to the registry, by periodic controls by the hepatologists and through telephones calls by the coordinator nurse, both before and after the transplantation. Every patient who dies during the 5 years of follow up will count as an event. Patients who are lost to follow up will be censored, in this case we will use the date of the last control or telephone call where he or she was alive.
次要结局
- Time to retransplantation(5 years)
研究者
Liliana Paloma Rojas Saunero
Research fellow
Hospital El Cruce