Clinical trial Recruiting at 1 site Observational Ages 18 to 75

Understanding gastric cardia vs non-cardia cancer using multiomics

Official title: Exploring the Difference Between Gastric Cardia Cancer and Non-cardia Gastric Cancer Based on Multiomics

Run by Qilu Hospital of Shandong University · NCT05812287 · Data updated 2026-11-12

Researchers are testing whether a multiomics approach can tell apart gastric cardia cancer from non-cardia gastric cancer in adults who have confirmed gastric cancer.

More Stomach Neoplasm trials

Quick facts

Study typeObservational
Ages18 Years to 75 Years
SexAll
Enrollment120 (estimated)
SponsorQilu Hospital of Shandong University
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Jinan, Shandong)
StatusRecruiting
StartedMarch 14, 2024
Main results expectedJune 2028
Study endsDecember 2028
Registry record updatedSeptember 8, 2026
Trial IDNCT05812287 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18-75 with pathologically confirmed gastric cancer (including high-grade intraepithelial neoplasia, early gastric cancer, and advanced gastric cancer) who can provide informed consent.

Probably not a fit

Patients who have had GI surgery in the past year, recently used certain GI medications or hormones, or have infections or other digestive diseases that interfere with results may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational case-control study that collects clinical data and multiple biological samples (saliva, serum, tissue, and feces) from participants with gastric cancer and matched controls. The goal is to identify molecular differences between cardia and non-cardia tumors using combined omics analyses. Participants are adults aged 18-75 who have a confirmed pathological diagnosis and have not had recent gastric surgery or treatments that could confound results. Samples and data will be analyzed to see if multiomics signatures can support early screening distinctions between the two cancer subtypes.

Why it matters

Potential benefit: If successful, the study could lead to better early screening and classification between cardia and non-cardia gastric cancers.

How similar studies have gone: Prior studies have shown that multiomics approaches can reveal distinct molecular patterns in cancer subtypes, supporting the novelty but with expected variability across cohorts.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Study population signing informed consent form
* Age: 18-75 years old
* The study population must underwent endoscopic examination and was confirmed by pathological diagnosis as gastric cancer: including high-level intraepithelial neoplasia, early gastric cancer, and advanced gastric cancer.

Exclusion Criteria:

* Those who have undergone gastrointestinal surgery within the past 1 year; Patients who have undergone neoadjuvant chemotherapy and have developed tumors in the residual stomach after previous partial gastrectomy.
* Those who have used proton pump inhibitors, antibiotics, probiotics, and prebiotics daily within the past month, and those who have recently received hormone therapy.
* People with infectious diseases and other digestive system diseases that interfere with the experimental results, such as inflammatory bowel disease, irritable bowel syndrome, etc.

Where it's running

  • Qilu Hospital of Shandong University
    Jinan, Shandong, China
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.