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NCT06370143Recruiting

A Study Collecting Health Information to Understand and Prevent Gastric Cancer

Gastric Cancer Prevention: Understanding Precursor Lesions and Risk Factors for Progression to Cancer

Source: ClinicalTrials.gov · Last updated 30 Jan 2026

Brief summary (registry, in English)

The purpose of this study is to create a registry of participants with precursor lesions for gastric cancer, including gastric atrophy, intestinal metaplasia, and dysplasia. Normal controls and individuals with gastric cancer for comparison of baseline characteristics will also be enrolled.

Status (registry)
Recruiting
Study type
Observational
Enrollment
3200 (estimated)
First submitted
12 Apr 2024
Start date
11 Apr 2024
Primary completion date
11 Apr 2036
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT06370143

What you commit to

  • Study type: Observational
  • Planned participants: 3200
  • From 11 Apr 2024 to the primary completion date, 11 Apr 2036
  • 7 sites 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

  • Individuals with a prior history of upper gastrointestinal surgery or a prior cancer who are undergoing active treatment for malignancy or have been diagnosed within 1 year prior to the study enrollment or with pancreatic cancer. (This does not include incidentally diagnosed primary gastric adenocarcinoma identified during study follow up. Individuals diagnosed with gastric carcinoid limited to the stomach will also be included, given their ongoing parallel risk for gastric adenocarcinoma.)
  • Individuals having Hereditary Diffuse Gastric Cancer Syndrome, mutations including CDH1 and CTNNA1, or more than one genetic mutation
  • Exclude high risk esophageal and duodenal lesions including:
    • Duodenal Adenoma
    • Dysplasia or cancer at the esophagus or gastroesophageal junction
  • Patients with an increased risk for biopsies during EGD, such as those with clotting disorders.

Age

  • Age \< 18 years old
  • Have severe comorbidities with expected survival time \<2 years or which would prevent them from undergoing routine elective EGD (at the discretion of the patient's provider and the study team)

Other

  • Women who are pregnant (may be enrolled after delivery)

Who the study is looking for

  • Age ≥ 18 years old
  • Able to read and understand English and Spanish
  • Meet criteria for one of three potentially eligible study populations:
    • Individuals with gastric atrophy, gastric intestinal metaplasia, or dysplasia: Had a previous diagnosis of or have been diagnosed by the investigation team with gastric atrophy, gastric intestinal metaplasia, or dysplasia of the gastric mucosa on pathology review from an endoscopic biopsy. Individuals who have a prior history of early gastric cancer may be included, if they were treated endoscopically and have no evidence of disease. Individuals who have a prior history of a cancer other than upper gastrointestinal cancer may also be included, if they have no evidence of disease for at least 1 year prior to study enrollment and are not undergoing active treatment for any malignancy at any time throughout the study period
    • Healthy controls (average risk): Individuals with no history of cancer or gastric precursor lesions undergoing a clinically indicated endoscopy at MSK for workup or dyspepsia or reflux
    • Gastric cancer cases: Individuals with a known diagnosis of early gastric adenocarcinoma undergoing surgical resection at MSK

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

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

SiteCityCountrySite status
Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities)
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesRecruiting
Memorial Sloan Kettering Suffolk-Commack (Limited protocol activity)
Coordinator of this site? Confirm its status
CommackUnited StatesRecruiting
Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Coordinator of this site? Confirm its status
HarrisonUnited StatesRecruiting
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Coordinator of this site? Confirm its status
MiddletownUnited StatesRecruiting
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Coordinator of this site? Confirm its status
MontvaleUnited StatesRecruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activites)
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Memorial Sloan Kettering Nassau (Limited Protocol Activites)
Coordinator of this site? Confirm its status
Rockville CentreUnited StatesRecruiting

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