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NCT07438418Not yet recruiting

An Observational Study on Gastric Cancer in High-risk Individuals

Risk of Gastric Cancer in High-risk Individuals: an Observational Cohort Study

Source: ClinicalTrials.gov · Last updated 27 Feb 2026

Brief summary (registry, in English)

This study is designed as a prospective observational cohort study, aiming to assess the differences in the occurrence of gastric cancer and the progression of gastric cancer-related precancerous lesions between individuals who test positive or negative for fecal multi-target testing, with baseline negative gastric endoscopy results. The clinical outcomes between the two groups will be compared through long-term follow-up.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
3000 (estimated)
First submitted
23 Feb 2026
Start date
31 Jan 2026
Primary completion date
1 Jul 2028
Lead sponsor
Fudan University
NCT number
NCT07438418

What you commit to

  • Study type: Observational
  • Planned participants: 3000
  • From 31 Jan 2026 to the primary completion date, 1 Jul 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • A history of diagnosed gastric cancer or other malignant tumors of the digestive tract.
  • Comorbid severe underlying conditions (e.g., severe cardiopulmonary insufficiency, liver or renal failure, etc.) that are likely to result in a short life expectancy or render long-term follow-up impractical.
  • Severe mental illness or incapacity to participate in the study due to lack of civil behavior.
  • Other conditions that the investigator deems inappropriate for participation in the study.

Other

  • Pregnant or breastfeeding women.

Who the study is looking for

  • Age ≥ 40 years, gender is not limited.
  • Able and willing to provide informed consent and willing to undergo baseline and follow-up examinations.

Age in the registry: 40 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
People's Hospital of Tongling City
Coordinator of this site? Confirm its status
TonglingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.