Actively Recruiting
The GAstric Precancerous Conditions Study
Led by Stanford University · Updated on 2025-12-16
600
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Gastric cancer affects about 27,000 Americans each year and often has a poor outlook because it is usually diagnosed late, when surgery to cure the cancer is less likely to succeed. This research studies patients at higher risk for gastric cancer, including those with precancerous changes in the stomach lining, such as atrophic gastritis and intestinal metaplasia. Both patients who have symptoms like indigestion and those without symptoms but with risk factors or known precursors are included. The study is observational and recruits patients from an endoscopy unit to better understand how these precancerous conditions change over time. Participants undergo outpatient endoscopy as part of their regular care, and researchers collect samples such as blood, saliva, and stomach tissue during these procedures. The study follows patients long-term to observe changes in their stomach tissue, looking for progression or improvement of the precancerous lesions. The main focus is to track changes using specific scoring systems (OLGA and OLGIM) and to monitor for the development of dysplasia or cancer over at least two years. During the study, participants provide biospecimens at their initial and follow-up endoscopies. Researchers assess tissue changes histologically and monitor participants for any signs of worsening or improvement. The study may continue for multiple years, with evaluations planned at least 24 months after enrollment. This long-term follow-up helps to understand risk factors and disease progression in people with gastric precancerous conditions.
CONDITIONS
Brief Title
The GAstric Precancerous Conditions Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects between 35 and 84 years old
- Undergoing outpatient endoscopy for abdominal pain, dyspepsia, iron deficiency anemia, Helicobacter pylori assessment, surveillance of suspected or known intestinal metaplasia, or evaluation for family history of gastric cancer
You will not qualify if you...
- Unable to give informed consent
- History of gastric surgery
- History of solid tumor or bone marrow transplant
- Platelet count less than 70 or international normalized ratio greater than 1.5
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single event at enrollment
Participants undergo outpatient endoscopy to detect precursor lesions and assess gastric precancerous conditions.
1 visit (in-person)
Duration - At least 24 months
Participants with precursor lesions are observed over time to monitor histologic progression, regression, and development of dysplasia or carcinoma.
Follow-up visits as scheduled by their healthcare provider
Trial Site Locations
Total: 1 location
1
Stanford University
Stanford, California, United States, 94305
Actively Recruiting
Research Team
R
Robert J Huang, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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