Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID06118437

Establishment and Validation of a Clinical Predictive Model for Gastrointestinal Cancer Screening Based on Patient-related Risk Factors: a Prospective, Multicenter Cross-sectional Study

Led by Air Force Military Medical University, China · Updated on 2025-07-24

1550

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Gastrointestinal tumors, including esophageal, gastric, and colorectal cancers, pose a serious health threat due to their high incidence and cancer-related mortality. Early detection through digestive endoscopy can significantly improve prognosis, with early-stage tumors having a five-year survival rate of up to 90%, compared to less than 30% for late-stage tumors. This research aims to identify the combined risk factors for these cancers and establish a predictive model for screening based on patient-related factors such as age, gender, family history, smoking, and alcohol use. This prospective, multicenter, cross-sectional observational study enrolls adults aged 18 to 80 who are undergoing both gastroscopy and colonoscopy. The study does not involve experimental treatments but focuses on collecting patient data to understand the overall risk factors associated with gastrointestinal tumors and develop a comprehensive risk prediction model. Participants will be assessed during their screening procedures, with data collected on their risk factors and health status. The primary outcome measured is the overall detection rate of gastrointestinal cancer over a two-year period. Researchers will analyze this data to improve early screening strategies. Participation involves no treatment intervention, but thorough information gathering during endoscopic examinations and follow-up over time.

CONDITIONS

Brief Title

Establishment and Validation of a Clinical Predictive Model for Gastrointestinal Cancer Screening Based on Patient-related Risk Factors

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 18 to 80 years
  • Undergoing both gastroscopy and colonoscopy simultaneously
Not Eligible

You will not qualify if you...

  • History of esophageal, gastric, or colorectal cancer
  • Suspected gastrointestinal obstruction or perforation
  • History of gastrointestinal tract surgery
  • Not suitable for endoscopic examination due to serious diseases or unstable hemodynamics
  • Unavailable relevant information
  • Pregnancy or lactation period
  • Unavailable informed consent form

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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 - 1 day

Participants undergo gastroscopy and colonoscopy to assist in the clinical predictive model for gastrointestinal cancer screening.

1 visit (in-person)

Long-term Monitoring

Duration - 2 years

Participants are monitored to observe the overall detection rate of gastrointestinal cancer over 2 years.

Periodic assessments over 2 years

Trial Site Locations

Total: 1 location

1

Xijing of Digestive Diseases

Xi'an, Shaanxi, China

Actively Recruiting

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Research Team

Y

Yang lin Pan, 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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Published Research Related To This Trial

Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.

Hyuna Sung, Jacques Ferlay, Rebecca L Siegel...

https://pubmed.ncbi.nlm.nih.gov/33538338