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Microbiome Test for the Detection of Colorectal Polyps

2021年9月19日 更新者:Biotax Labs LTD

The main goal of this trial is to validate a new method for colorectal polyp screening based on stool microbiome signatures. 600 Individuals who are scheduled / planned to undergo a colonoscopy will be recruited for this study and a stool sample and an optional saliva sample will be collected.

Analyze process will be conducted on the microbiome of the samples given.

研究概览

地位

招聘中

条件

详细说明

Colorectal cancer (CRC) is the second cause of cancer death in the US. The pathogenesis of CRC is complex, involving a progressive transition of the healthy colonic mucosa to pre-cancerous polyps, and eventually to CRC. One of the factors that are proposed to cause this 'adenoma-carcinoma sequence' is the dysbiosis of the gut microbiome.

The gut microbiota has been identified as a potential screening biomarker for CRC, since studies have reported specific bacterial taxa and/ or microbial signatures as important factors in the etiology of CRC.

Hypothesis:

comprehensive and cutting-edge metagenomic analysis of the fecal microbiome of individuals with colonic polyps vs. patients without polyps will identify microbial signatures associated with colonic polyps and will define these microbial signatures as biomarkers and risk factors for CRC.

method:

  • Collect data (anthropometric, demographic, dietary, lifestyle habits, medical and family history) and stool & optional Saliva sample for microbiome analysis from a cohort of 600 colonoscopies screened individuals.
  • Analyze this data with an aim to utilize advanced artificial intelligence and machine-learning techniques to classified microbiome signatures, which are correlated to colonoscopy (and to histological) results.
  • Blinded Validation - A sub-cohort of 300 individuals (who are part of the 600 individuals) that were not used to classify the biomarkers signatures will be used to validate the diagnosis model.

Data analysis:

The stool and optional Saliva samples will be sent to metagenomic sequencing, thereby generating FASTQ libraries of the reads found in the stool & saliva samples. These files will be analyzed by the BiotaX diagnostics platform.

No Human DNA analysis will take place at this clinical study. Only a microbial analysis will take place.

研究类型

介入性

注册 (预期的)

600

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Shay Hilel
  • 电话号码:+972-54-4386721
  • 邮箱shay@biotax.co

研究联系人备份

  • 姓名:Naama Geva-Zatorsky, Ph.D
  • 电话号码:+972-52-292-2300
  • 邮箱naamagz@biotax.co

学习地点

      • Haifa、以色列
        • 招聘中
        • Rambam Medical Center
        • 接触:
          • Erez Hasnis, MD
      • Tel Aviv、以色列
        • 招聘中
        • Assuta Medical Center
        • 接触:
          • Zohar Levi, MD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

45年 至 70年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Males or females.
  2. Age: 45-70 years, inclusive.
  3. Patients without any incapacitating systemic disease
  4. Able to comprehend and provide informed consent.
  5. Patients who are scheduled / planned to undergo a colonoscopy, preferably: participants who are undergoing a colonoscopy as a diagnostic surveillance.

Exclusion Criteria:

  1. Subject has a history of colorectal cancer (CRC)
  2. Subject has a diagnosis or medical history of any of the following conditions:

    • Familial adenomatous polyposis (also referred to as "FAP", including attenuated FAP and Gardner's syndrome)
    • Hereditary non-polyposis CRC syndrome (also referred to as "HNPCC" or "Lynch Syndrome")
  3. Subject has a diagnosis or personal history of inflammatory bowel disease (IBD), including chronic ulcerative colitis or Crohn's disease.
  4. Patients with incapacitating systemic disease
  5. Any use of antibiotics within one months prior to colonoscopy.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:诊断
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:colonoscopy
Participants will be patients undergoing colonoscopy
patients who are scheduled to undergo colonoscopy will be asked to participate and give a stool sample

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
diagnose existence of colon polyps
大体时间:year
To determine whether fecal metagenomics microbial signatures can significantly predict adenoma\ sessile serrated polyps (SSP) existence in patients and serve as diagnostic biomarkers.
year

次要结果测量

结果测量
措施说明
大体时间
diagnose sub types of colon polyps
大体时间:year
To determine whether fecal metagenomics microbial signatures can significantly identify between the following subgroups: non-polyp group, Hyperplastic polyps, adenomas - <5 mm, 6-10mm polyp group and >10mm polyp group.
year
Saliva microbiome vs stool microbiome
大体时间:year
To determine if Saliva microbiome sample can provide indication same as Stool microbiome sample.
year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Zohar Levi, MD、Assuta Medical Center
  • 首席研究员:Erez Hasnis, MD、Rambam Health Care Campus

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年7月27日

初级完成 (预期的)

2022年7月1日

研究完成 (预期的)

2022年12月1日

研究注册日期

首次提交

2021年9月19日

首先提交符合 QC 标准的

2021年9月19日

首次发布 (实际的)

2021年9月29日

研究记录更新

最后更新发布 (实际的)

2021年9月29日

上次提交的符合 QC 标准的更新

2021年9月19日

最后验证

2021年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • Biotax_001

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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