跳至主要内容
临床试验/NCT05824403
NCT05824403招募中不适用

PAncreatic Disease Cohort of TOuLouse

University Hospital, Toulouse1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2023年11月28日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
300
试验地点
1
主要终点
Diagnostic tools

研究概览

简要总结

This study is a prospective cohort dedicated to pancreatic diseases excluding cancer. The aim is to develop positive or differential diagnostic tools between benign potentially malignant or malignant pancreatic pathologies. During this study the investigators collect data and biological samples to support research project.

详细描述

This collection focuses on pathology of the pancreas requiring specific investigations or management for diagnosis or treatment. Pancreatic pathologies can be classified as malignant, potentially malignant or benign tumors. These can be solid or cystic. There is an inflammatory attack on the pancreas, generating acute pancreatitis in the acute period, if the inflammatory manifestations persist, chronic pancreatitis will develop. Some lesions may be at risk of malignancy during their evolution, it is therefore necessary to improve the performance of monitoring and diagnostic tools in order to adapt the management of patients.

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

入选标准

  • Patients with inflammatory or cystic exocrine pancreatic pathology
  • Patient able to read and understand the information leaflet
  • Patients who have agreed to participate in the study and have signed the free and informed consent
  • Patients affiliated to a social security system (including AME)

排除标准

  • Patient with pancreatic cancer pathology
  • Patients with active cancer, whatever the origin
  • Pregnant or breastfeeding patients
  • Patients under legal protection, guardianship or trusteeship

结局指标

主要结局

Diagnostic tools

时间窗: 3 years after the first inclusion

To develop positive or differential diagnostic tools between benign potentially malignant or malignant pancreatic pathologies

次要结局

  • Microbiota(3 years after the first inclusion)
  • New targets(3 years after the first inclusion)
  • Improvement of management(3 years after the first inclusion)
  • Clinical data access(3 years after the first inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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