Actively Recruiting

Age: 19Years - 100Years
All Genders
ID04665687

Clinical Sequencing Project for Early Gastric Cancer and Precancerous Gastric Adenoma Patients for Personalized Cancer Clinic

Led by Samsung Medical Center · Updated on 2025-09-12

1730

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying early gastric cancer and precancerous gastric adenoma to improve diagnosis and predict recurrence. These conditions have a high cure rate when detected early, often treatable by endoscopic removal, which helps maintain a good quality of life. However, there are currently no markers available to diagnose early gastric cancer or predict its return after treatment. The study collects tumor tissue and blood samples from patients diagnosed with early gastric cancer or gastric adenoma at different times: initially, 2 months, 1 year after treatment, and if recurrence occurs. Advanced genetic testing methods, including targeted sequencing and copy number variation analysis, are used to profile tumors. Additional tests include immunohistochemistry and cancer-specific scans to analyze molecular changes. Participants will undergo sample collection and molecular profiling over up to 2 years to identify biomarkers that help diagnose and predict cancer recurrence. Researchers will review genetic changes over time and measure disease-free survival. The goal is to gather detailed molecular information to support personalized care for these patients.

CONDITIONS

Brief Title

Clinical Application of Genetic Sequencing of Early Gastric Cancer and Gastric Adenoma Patients

Who Can Participate

Age: 19Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 19 years or older
  • Histologically confirmed diagnosis of early gastric cancer or precancerous gastric adenoma
  • Availability of excess tissue from previous biopsy or endoscopic treatment for research
  • Life expectancy greater than 3 months
  • Voluntary consent to participate in the clinical trial
Not Eligible

You will not qualify if you...

  • Insufficient sample quantity for analysis
  • Considered unsuitable for the study by the researchers

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - At initial treatment

Participants provide tumor tissue and blood samples for genomic examination and molecular profiling at the time of initial treatment.

1 baseline visit (in-person)

Long-term Monitoring

Duration - Up to 2 years or until recurrence

Participants provide additional tissue and blood samples at 2 months, 1 year after treatment, and at recurrence to observe changes in tumor molecular profile and to identify biomarkers for diagnosis and prognosis.

3 follow-up visits (in-person) at 2 months, 1 year, and at recurrence if applicable

Trial Site Locations

Total: 1 location

1

Samsung medical center

Seoul, South Korea

Actively Recruiting

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Research Team

C

Clinical Research Coordinator

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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