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Clinical Trials in China / NCT07793110
Starting soon Observational

Early Diagnosis Model of Colorectal Adenoma Using Laboratory Examinations

NCT07793110 · tracked via the Priya Life Science China tracker
Sponsor
Renmin Hospital of Wuhan University
Phase
Observational
Started
2026-09-01
Last updated
2026-08-28

Condition(s) studied

Colorectal AdenomaPolyp

Investigational drug(s) / intervention(s)

No active intervention

No active intervention: This is an observational cohort study. No drugs, surgical procedures or therapeutic interventions will be provided to participants. Only routine clinical laboratory and demographic data are collected for constructing and validating a prediction model for colorectal adenoma.

Study summary

Colorectal cancer has the third highest incidence and second highest mortality rate of all malignant tumors worldwide. Distinct from most other cancers, colorectal cancer can be prevented; colonoscopy-based identification and removal of adenomatous polyps is the most effective preventive measure. Early intestinal adenomas rarely cause specific symptoms, and many patients are diagnosed at advanced stages once symptoms emerge, leading to unsatisfactory treatment and prognosis. Colonoscopy, the main diagnostic tool for intestinal adenoma, is invasive, resulting in limited patient compliance, while grassroots hospitals face shortages of medical resources. There is an urgent demand for a convenient, affordable and well-tolerated early diagnostic method for intestinal adenoma. Artificial intelligence techniques can efficiently analyze routine clinical laboratory data. This study aims to establish an AI-based predictive model combining clinical information and laboratory test results to realize early identification of intestinal adenoma and optimize patient prognosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
Accepted
Inclusion Criteria: * Patients aged ≥ 18 years undergoing colonoscopy, with pathologically confirmed diagnosis of colorectal adenoma or non-adenomatous lesions (e.g., inflammatory polyps, hyperplastic polyps, chronic inflammation, etc.); * Capable of reading, understanding and signing the informed consent form; * The investigator judges that the subject can understand the procedures of this clinical study, and is willing and able to cooperate with and complete all study procedures. Exclusion Criteria: * Unavailable clinical data including laboratory test results; * Neoplastic lesions other than colorectal adenoma; * Non-first diagnosis of colorectal adenoma; * Autoimmune diseases; * Repeated enrolled subjects (duplicate patients); * Pregnancy or breastfeeding status; * Failure to obtain informed consent; * The investigator considers that the subject has high-risk diseases or other special conditions unsuitable for participating in this clinical trial.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Renmin Hospital of Wuhan University Wuhan Hubei

More Renmin Hospital of Wuhan University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07793110 on ClinicalTrials.gov ↗ ← All trials in China