Post-operative Monitoring of Gastric Cancer

Launched by SUZHOU HUHU HEALTH & TECHNOLOGY INC. · Jun 15, 2025

Keywords

ClinConnect Summary

This clinical trial is studying a new, simple way to keep track of stomach (gastric) cancer after surgery using a special test that looks for certain markers in the body without needing invasive procedures. The goal is to see how well this new test works in monitoring patients who have had surgery for gastric cancer.

Adults over 18 who have stomach discomfort and are visiting the Gastric Surgery Department at the study center may be eligible to join, especially if they have had or will have a gastroscopy (a procedure where a thin tube with a camera looks inside the stomach) or tissue tests done there. People with serious health problems like heart, liver, or kidney issues, previous cancer, certain infections, or those already receiving specific immune-related treatments cannot join. Participants will be asked to provide samples for the test and will need to understand and sign a consent form. This study is currently enrolling patients and aims to help find easier, less invasive ways to monitor gastric cancer after surgery.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Subject age over 18.
• • 2. Subject has stomach discomfort, and seek medical attention at the Gastric Surgery Department of our center.
• • 3. Subject has or will have gastroscopy and/or pathological examination results at this center.
• • 4. Subject must be able to fully understand the informed consent form and be able to personally sign it.
• Exclusion Criteria:
• • 1. Subject has serious heart, liver, kidney dysfunction, or mental illness.
• • 2. Subject diagnosed previously with any kind of malignant tumor.
• • 3. Subject is known to be infected with HIV or other related diseases (considering interference from the use of immune drugs).
• • 4. Subject is receiving targeted drugs, immunosuppressants, immunomodulators, and biological therapies.
• • 5. Researchers believe that subject is not suitable for enrollment.
• • 6. Subject can not supply sufficient sample to complete this experiment.