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The analysis of the clinicopathological characteristics of traditional serrated adenoma

The analysis of the clinicopathological characteristics of traditional serrated adenoma

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103019
Enrollment
Unknown
Registered
2025-05-22
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traditional serrated adenoma

Interventions

The traditional serrated adenoma group:None
The traditional serrated adenoma with dysplasia group:None

Sponsors

The second hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The full colonoscopy was complete; 2. The patient was detected with polyps by colonoscopy and was pathologically diagnosed as a traditional serrated adenoma.

Exclusion criteria

Exclusion criteria: 1. The patient also has other intestinal diseases: inflammatory bowel disease, hereditary colorectal cancer (the first type is non-polyposis syndrome, including Lynch syndrome and familial colorectal cancer X Lynch syndrome; The second category is polyposis syndrome, including familial adenomatous polyposis, etc. ; 2. The patient was diagnosed with a history of colorectal malignant tumors and malignant tumors in other parts before microscopic examination; 3. The patient has a history of colorectal resection and advanced adenoma resection; 4. The colonoscopy of the patient was incomplete, failing to reach the cecum, and the intestinal preparation was unqualified (Boston score <6 points).

Design outcomes

Primary

MeasureTime frame
Endoscopic data;Pathological data;Endoscopic treatment methods;Multi-omics;

Secondary

MeasureTime frame
General information;

Countries

China

Contacts

Public ContactHonglei Wu

The second hospital of Shandong University

whl20011996@163.com+86 176 6008 0767

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026