Blood test may reveal stomach cancer before symptoms

NCT ID NCT07782294

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 24, 2026 · Last updated Aug 25, 2026 · Updated 1 time

Summary

This trial is testing whether a new blood test that looks at DNA in red blood cells, aided by artificial intelligence, can accurately detect stomach cancer. It will involve about 542 adults scheduled for an upper endoscopy to check for stomach conditions. The test's accuracy will be compared to standard methods like tumor markers and H. pylori testing, using biopsy results as the gold standard.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
An AI-assisted blood test that analyzes DNA from red blood cells (rbcDNA) to detect gastric cancer.
What this could lead to
If successful, this blood test could offer a simple, non-invasive way to catch gastric cancer earlier, potentially improving survival odds.
What could go wrong
This is a validation study, so the test's accuracy is not yet proven. It may not outperform existing methods, and false positives or negatives remain possible.

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

About 542 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

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

Participants consist of patients with gastric diseases undergoing gastroscopy, enrolled from three different medical centers across China.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria * Age between 18 and 75 years. * Scheduled for upper gastrointestinal endoscopy for the assessment of gastric diseases, including gastric cancer (stage I-IV), gastric precancerous lesions, and other benign gastric disorders. * No previous treatment for the current gastric disease prior to blood collection, including surgery, chemotherapy, radiotherapy, immunotherapy and other anti-tumor therapies. * Able and willing to participate and provide written informed consent. Exclusion Criteria * Receiving therapeutic gastroscopy or endoscopic resection for gastric lesions diagnosed in other institutions. * Presence of conditions that hinder complete gastric endoscopic visualization and reliable lesion evaluation, such as gastric retention and severe esophageal stenosis. * History of other malignant tumors, prior anti-tumor treatment, or partial/total gastrectomy. * Severe hemodynamic instability, malignant arrhythmia, unstable cardiovascular diseases, or recent major surgery. * Hematological disorders, recent blood transfusion history, severe active infection, chronic infectious diseases (e.g., HIV), or severe systemic inflammation affecting blood cell composition. * Pregnant or breastfeeding women. * Enrolled in other concurrent clinical trials that may affect the current study results. * Refusal to sign informed consent or failure to comply with study procedures.

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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.

  1. The places running it

    3 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Anyang Tumor Hospital

    Anyang, Henan, 455000, China

  • Renji Hospital, Shanghai Jiaotong University School of Medicine

    Shanghai, 200001, China

  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    Hangzhou, Zhejiang, 310009, China

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