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Completed

NCT Number: NCT03146520

Clinical Validation of Stool DNA-based SDC2 Methylation Test for Colorectal Cancer Detection

Pivotal trials of SDC2 methylation biomarker test in stool DNA to estimate clinical sensitivity and specificity in detection of colorectal cancer.

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Key information

About this study

The purpose of this study is to validate the clinical performance of EarlyTect Colon Cancer test which is measuring Syndecan 2 methylation status in stool DNA to detect CRC. Syndecan 2 (SDC2) is a newly developed methylation biomarker for colorectal cancer diagnosis. Methylation status of SDC2 gene in stool DNA is determined by methylation specific qPCR. Sensitivity and specificity will be determined by comparing Stool DNA test from healthy subjects, CRC patients, and other group including polyps and other diseases.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • sample information is complete, including sample number, gender, family history, stage of cancer, treatment history, and other disease information
  • the CRC patient who has not any treatment (surgery, chemotherapy, or radiation)
  • non-CRC patient who has not received any treatment (surgery, chemotherapy, or radiation) within the last 6 months
  • all of above conditions are satisfied, and any one of below can be applicable; 1) confirm to be CRC with colonoscopy and/or pathological examination, 2) confirm to be inflammatory or ulcerative bowel diseases or benign hyperplastic polyp, 3) confirm to be gastrointestinal or liver cancers who are not CRC, 4) schedule to receive colonoscopy and additional confirmation test for CRC with agreement to provide the test results.

Exclusion criteria

any one of below can be applicable;

  • the patient information is not complete and/or does not satisfy inclusion criteria
  • the sample information is not complete and/or does not satisfy inclusion criteria
  • the CRC patient who has history of colorectal cancer surgery, chemotherapy, or any other treatment
  • non-CRC patient who received any chemotherapy within the last 6 months
  • the patient who has limited ability or are vulnerable to accept clinical trial agreement
  • the patient who is judged as not suitable for clinical trial including a psychiatric disorder by a physician

Treatment and study plan

EarlyTect Colon Cancer

Device

SDC2 methylation assay by qPCR using EarlyTect Colon Cancer kit

Primary outcomes

  1. Clinical performance of EarlyTect Colon Cancer to detect colorectal cancer

    Time frame: 1.5 years

    Sensitivity and specificity of EarlyTect Colon Cancer to detect colorectal cancer (sensitivity: the ratio of positive cases in all CRC cases, specificity: the ratio of negative cases in all healthy controls)

Secondary outcomes

  1. Positive ratio of SDC2 methylation in polyps

    Time frame: 1.5 years

    the ratio of SDC2 methylation positive in polyps

  2. Positive ratio of SDC2 methylation in other cancers

    Time frame: 1.5 years

    the ratio of SDC2 methylation positive in other cancers

Sponsors and collaborators

Lead sponsor

Genomictree, Inc.

Industry

Collaborators

  • Severance Hospital

Registry information

Official study title

Clinical Study for the Validation of Real Time qPCR for SDC2 Methylation in Stool DNA for Early Detection of Colorectal Cancer

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
May 10, 2017
Registry last updated
Apr 18, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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