Actively Recruiting

Age: 20Years +
All Genders
Healthy Volunteers
ID05291728

Screening for Early Gastric Cancer in Shaanxi Province

Led by Second Affiliated Hospital of Xi'an Jiaotong University · Updated on 2022-03-23

12500000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting an observational study to screen for early gastric cancer among local residents aged over 20 years in 11 regions of Shaanxi Province. The study aims to evaluate the prevalence of dyspepsia, gastroesophageal reflux disease, precancerous lesions, and Helicobacter pylori infection in this natural population. A new gastric cancer risk assessment model will be developed based on the collected data. Participants provide basic information through questionnaires covering social demographics, lifestyle, and medical history. Serum Helicobacter pylori antibody tests are also performed. The expert group then identifies individuals at high risk for gastric cancer, who, if they have no contraindications, undergo electronic gastroscopy in designated hospitals after informed consent. Throughout the study, data on symptoms, infections, treatments, and recurrence rates are collected and analyzed. The primary outcome is the detection rate of early gastric cancer over the six-year period from October 2020 to October 2026. Secondary outcomes include the prevalence of digestive conditions and infection rates. This comprehensive approach helps understand risk factors and disease prevalence in the population.

CONDITIONS

Brief Title

Screening for Early Gastric Cancer in Shaanxi Province

Who Can Participate

Age: 20Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Local resident over 20 years old
  • Provided verbal informed consent to participate
Not Eligible

You will not qualify if you...

  • Refused to participate in this research project
  • Did not complete questionnaires or serological tests for Helicobacter pylori antibodies
  • Study participation was not completed due to other reasons

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 - From October 2020 to October 2026

Participants complete questionnaires about their social and health background and undergo serological testing for Helicobacter pylori antibodies. High-risk participants undergo electronic gastroscopy in designated hospitals.

Questionnaire and blood test at 1 visit; gastroscopy for high-risk participants (1 visit in-person)

Long-term Monitoring

Duration - From October 2020 to October 2026

Participants are observed for the prevalence of digestive diseases and outcomes related to Helicobacter pylori infection, including treatment and recurrence rates.

Data collected periodically during the study period

Trial Site Locations

Total: 1 location

1

The second affiliated hospital of xi'an jiaotong university

Xi'an, Shaanxi, China, 710004

Actively Recruiting

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Research Team

J

jinhai Wang, MD

R

Rui Wang, MD

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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