NCT07561814招募中不适用
A Study on a Predictive Model for Efficacy and Prognosis of Pancreatic Carcinoma Based on Multimodal Data
Shanghai Zhongshan Hospital1 个研究点 分布在 1 个国家目标入组 1,030 人开始时间: 2025年12月9日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 1,030
- 试验地点
- 1
- 主要终点
- overall survival
研究概览
简要总结
The goal of this observational study is to learn if combining information from CT scans, blood tests, and pathology reports can better predict how pancreatic cancer will progress.
The main questions it aims to answer are:
- Can combining these types of data more accurately estimate how long a person might survive?
- Can it better predict the risk of recurrence?
Participants will not have any extra tests or treatments. They will:
- Allow researchers to collect information from their existing medical records (such as surgery reports, imaging, and lab results)
- Receive a follow-up phone call for up to 3 years to share health updates（about every 3 months for the prospective cohort）.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
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
- •Age ≥ 18 years.
- •Histologically or cytologically confirmed diagnosis of pancreatic cancer.
- •Availability of preoperative and postoperative contrast-enhanced CT images at the participating center; patient records include corresponding clinical data, postoperative pathological reports, and preoperative and postoperative blood test results.
- •Underwent surgical treatment for pancreatic cancer at a participating center of this study.
排除标准
- •Age < 18 years (minors).
- •Presence of other severe diseases (e.g., severe liver or kidney failure, cardiovascular or cerebrovascular diseases, malignancies other than pancreatic cancer); pregnant or breastfeeding women; individuals with mental illness;
- •patients unable to comply with follow-up or provide informed consent.
- •Presence of significant outliers (e.g., laboratory values exceeding 10 times the normal range without clinically reasonable explanation) or samples with excessive missing data.
研究组 & 干预措施
prospective cohort
Retrospective cohort
结局指标
主要结局
overall survival
时间窗: 3 years
recurrence free survival
时间窗: 3 years
recurrence status within one year after surgery
时间窗: 3 years
次要结局
未报告次要终点
研究者
研究点 (1)
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