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临床试验/NCT05694845
NCT05694845尚未招募不适用

A Clinical Study Experiences of Cholangiocarcinoma Patients To Identify Trial Attributes Affecting Completion Rates For Specific Demographic Groups

Power Life Sciences Inc.0 个研究点目标入组 500 人开始时间: 2024年2月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
500
主要终点
Number of Cholangiocarcinoma patients who remain in clinical trial until completion.

研究概览

简要总结

The main reason for conducting this research is to gain a better understanding of why some people with cholangiocarcinoma are not able to participate in or complete clinical trials. Historically, certain groups of people have been more likely to participate in clinical trials, but there hasn't been much research to understand why this is the case.

The goal is to find out which aspects of a clinical trial may make it more difficult for patients to take part or see it through. The data will be evaluated through different demographic lenses and identify trends that could help improve the experience of future cholangiocarcinoma patients during clinical trials.

研究设计

研究类型
Observational
观察模型
Case Crossover
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

  • Patient is at least 18 years of age
  • Participant has a diagnosis of Cholangiocarcinoma
  • Patient has self-identified as planning to enroll in an interventional Cholangiocarcinoma clinical trial
  • Patient must provide written informed consent

排除标准

  • No diagnosis of Cholangiocarcinoma confirmed
  • Inability to perform regular electronic reporting
  • Women who are pregnant, intend to become pregnant, or are lactating
  • Patient does not understand, sign, and return consent form

结局指标

主要结局

Number of Cholangiocarcinoma patients who remain in clinical trial until completion.

时间窗: 12 months

Rate of patients who decide to enroll in a Cholangiocarcinoma Clinical Study.

时间窗: 3 months

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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