A cohort study assessing a blood test for early cancer detection in Nanjing
Official title: A Prospective, Multicenter Cohort Study of the Multi-omics Liquid Biopsy MCED Test MERCURY in an Average Risk Chinese Population
Run by Nanjing Shihejiyin Technology, Inc. · NCT06011694 · Data updated 2026-11-12
This study is testing a new blood test to see if it can detect different types of cancer earlier in people aged 45-75 in Nanjing, China.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 45 Years to 75 Years |
| Sex | All |
| Enrollment | 15000 (estimated) |
| Sponsor | Nanjing Shihejiyin Technology, Inc. Industry-sponsored |
| Locations | 2 sites (Nanjing, Jiangsu and 1 other locations) |
| Status | Recruiting |
| Started | June 15, 2022 |
| Main results expected | May 15, 2027 |
| Study ends | May 15, 2027 |
| Registry record updated | August 25, 2023 |
| Trial ID | NCT06011694 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals aged 45-75 residing in Nanjing who are willing to participate in the study procedures.
✕Probably not a fit
Patients with a history of cancer, current cancer diagnosis, or certain medical conditions may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The Jinling Cohort is a prospective, multicenter observational study involving 15,000 individuals aged 45-75 in Nanjing, China. Participants will undergo blood collection for the MERCURY multi-omics liquid biopsy test, complete health questionnaires, and annual physical exams over three years, followed by two additional years of follow-up. The study aims to evaluate the test's sensitivity, specificity, and predictive values, as well as its ability to detect multiple cancer types earlier than conventional methods. Additionally, it will assess participants' attitudes towards the MCED blood test.
Why it matters
Potential benefit: If successful, this study could lead to earlier detection of multiple cancers, potentially improving patient outcomes and reducing late-stage diagnoses.
How similar studies have gone: While similar approaches have been explored, the specific application of the MERCURY test in this cohort is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1、45-75 years of age; 2、Willing and able to undergo blood sample collection, health questionnaires and annual routine physical exams once a year for three consecutive years; 3、Residents in Nanjing; 4、Fully understand the study and able to provide a written informed consent Exclusion Criteria: 1. Pregnant women; 2. Individuals who have history of cancer or current diagnosis of cancer; 3. Individuals who have organ transplant or prior non-autologous (allogeneic) bone marrow or stem cell transplant; 4. Individulas who have blood transfusion within 30 days prior to the blood draw; 5. Individuals who have an acute infection or inflammation within 14 days prior to the blood draw; 6. Individuals who have taken medication with anti-tumor effects within 30 days prior to the blood draw; 7. Individuals who will not be able to comply with the protocol procedures judged by researchers
Where it's running
-
Nanjing Jiangbei People's Hospital
Nanjing, Jiangsu, China Recruiting -
The Fourth Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China Recruiting
Study contacts
- Principal investigator: Shao Yang, Ph.D — NanjingShihejiyin Technology Inc.
- Study coordinator: Shanshan Yang, Ph.D
- Email: admin@geneseeq.com
- Phone: 8613585145836
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.