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临床试验/NCT04180735
NCT04180735已完成不适用

Intestinal Perforation in Patients Receiving an Orthtopic Liver Transplantation in the Montpellier University Hospital: a Retrospective and Observational Study.

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Evaluate the total length of stay

研究概览

简要总结

Liver transplantation enhances the prognosis of patients with cirrhoses or hepatocellular carcinoma. However some patients develop intestinal perforations for which the prognosis is poor.

The aim of the study is to evaluate the risk factors of intestinal perforations using a retrospective study scheme.

详细描述

Liver transplantation enhances the prognosis of patients with cirrhoses or hepatocellular carcinoma. However some patients develop intestinal perforations for which the prognosis is poor.

The aim of the study is to evaluate the risk factors of intestinal perforations using a retrospective study scheme. Previous studies have shown a possible implication of drugs or medical history or intraoperative complications. The investigators aim to describe the other possible risk factors (such as portal vein clampage) and the type of surgery done after the diagnosis and its impact on survival as well.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients having received an orthotopic liver transplantation in the Montpellier University Hospital from 2014 to 2019
  • for the group Perforation: patients having during the follow-up a complication such as intestinal perforation. The complete list uses the ICD-10 codes for intestinal perforation, esophageal perforation, duodenal perforation etc.

排除标准

  • No exclusion criteria

结局指标

主要结局

Evaluate the total length of stay

时间窗: 6 months.

Evaluate the total length of stay

次要结局

  • Evaluate the number of perforations(1 month, 3 months, 6 months.)
  • Evaluate the occurrence of an acute or chronic rejection(1 month, 3 months, 6 months.)
  • Evaluate the occurrence of death(1 month, 3 months, 6 months.)
  • Evaluate the quality of life(1 month, 3 months, 6 months.)
  • Evaluate the total number of complications(1 month, 3 months, 6 months.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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