AI takes on esophageal cancer: could it spot the disease earlier?
NCT ID NCT07642401
First seen Jun 25, 2026 · Last updated Aug 28, 2026 · Updated 3 times
Summary
This study is testing whether an artificial intelligence (AI) model can help doctors better detect, diagnose, and treat esophageal cancer. Researchers will feed de-identified data from 12,000 patients receiving routine care into the AI and compare its recommendations to standard care over three years. The goal is to see if the AI can improve early detection rates and treatment personalization.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could show that AI helps doctors catch esophageal cancer earlier and choose better treatments, potentially improving survival rates.
- What could go wrong
- This is an observational study, not a controlled trial, so results may not prove cause and effect. The AI model may not work as well in real-world settings or for all patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 12,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population comprises patients receiving routine esophageal cancer management at participating healthcare institutions, including those undergoing screening (e.g., endoscopy), diagnosis (imaging, pathology), treatment (endoscopic resection, surgery, chemotherapy, radiotherapy), and prognostic follow-up. Inclusion criteria: age ≥18 years, suspected or confirmed esophageal cancer, and available complete clinical data (endoscopy, imaging, pathology, and follow-up records). Exclusion criteria: incomplete data or refusal to use medical records. The population spans early to advanced stages to evaluate the AI model across the full disease spectrum.
- Ages
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18 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 1\. Aged 18 years or older. 2. Individuals with normal findings or inflammatory changes: endoscopic or pathological reports indicating "no significant abnormalities detected" or changes consistent with inflammation. 3\. Individuals with benign lesions: pathological reports specifying "absence of tumor cells" or a diagnosis consistent with benign lesions. 4\. Individuals with precancerous lesions: pathological reports with a definitive diagnosis of Low-grade Intraepithelial Neoplasia (LGIN) or High-grade Intraepithelial Neoplasia (HGIN). 5\. Individuals with malignant tumors: pathological reports confirming a diagnosis of esophageal squamous cell carcinoma or esophageal adenocarcinoma. Exclusion Criteria: * 1\. Diagnostically uncertain: Lack of definitive pathological evidence, or with doubtful clinical diagnosis. 2\. Poor data quality: Low-quality key imaging data (endoscopy, CT) that is unsuitable for analysis (e.g., severe artifacts, missing images). 3\. Severe missingness of key clinical or follow-up data (missing rate \> 20%). 4. Confounding by other malignancies: Presence of other active malignant tumors other than esophageal cancer within 5 years prior to enrollment. 5\. Loss to follow-up: Failure to obtain key survival or recurrence follow-up information in the retrospective cohort.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Anyang Tumor Hospital
Anyang, Henan, 455000, China
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Nanyang Central Hospital Medical Ethics Committee
Nanyang, Henan, 473000, China
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The First Affiliated Hospital of Henan University of Science & Technology
Luoyang, Henan, 471000, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Swallowable capsule and lab test take on endoscopy for esophageal cancer screening
- Can a drug combo stop esophageal cancer from returning after surgery?
- Blood proteins may predict who beats esophageal cancer with chemoradiation
- Experimental drug put to the test against Hard-to-Treat GI cancers
- Can a drug combo shrink esophageal tumors before surgery?