Plain-English translation of NCT00260585 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a research registry — a long-term study where researchers collect blood samples, tissue samples, and health information from thousands of people. The goal is to understand what causes esophageal cancer and who is most at risk. By studying these samples and medical histories, scientists hope to find better ways to prevent and treat this disease.
Esophageal cancer is a serious disease, but doctors don't yet fully understand which people will develop it or why some people get it while others don't. This registry was created to gather enough information from many patients so researchers can identify patterns, risk factors, and warning signs that could lead to earlier detection and better treatment.
You likely qualify if…
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You'll be asked to complete a health questionnaire about your habits, medical history, and family medical history — usually during a clinic visit before any planned procedure. During or around the time of your surgery or endoscopy, researchers will collect a small blood sample (about 3 tablespoons) and may collect small tissue or fluid samples from your esophagus and stomach. Some samples are collected only once, while blood may be drawn again during routine follow-up visits. The entire process is integrated into your normal medical care.
AI-generated summary from trial data · Jun 4, 2026 · Not medical advice
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