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Not yet recruiting NCT07678788

Study on the Association Between Serrated Polyps and Metachronous Advanced Colorectal Neoplastic Lesions

Observational Sessile Serrated Lesion Serrated Polyp

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Sessile Serrated Lesion, Serrated Polyp. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Risk Factors for Metachronous Advanced Colorectal Lesions After Endoscopic Resection of Serrated Lesions

Overview

This study aims to explore the risk factors associated with the development of ACN and same-site ACN in patients with SP, thereby informing the optimization of clinical surveillance strategies

Primary outcome measures

  • The occurrence of metachronous ACN [Time frame: At least 6 months after index colonoscopy]

Eligibility criteria

Inclusion criteria

  • Adult patients aged > 18 years;At least one SP detected during the index colonoscopy and pathologically confirmed as TSA or SSL (according to the 2019 WHO classification criteria);Underwent complete polypectomy during the index colonoscopy;Received regular follow-up at Changhai Hospital, with an interval of ≥ 6 months between the index and follow-up colonoscopies;Complete clinical and pathological data.

Exclusion criteria

  • Incomplete colonoscopy or failed cecal intubation;Inadequate bowel preparation, defined as a Boston Bowel Preparation Scale (BBPS) score < 6 or a score < 2 in any bowel segment;Withdrawal time < 6 minutes;Diagnosis of hereditary cancer syndromes, such as familial adenomatous polyposis (FAP) or Lynch syndrome;Concurrent inflammatory bowel disease (IBD) or indeterminate colitis;History of colorectal cancer or other malignancies;Incomplete clinical or pathological records.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Publications

  • [1] SIEGEL R L, MILLER K D, JEMAL A. Cancer statistics, 2020[J/OL]. CA: A Cancer Journal for Clinicians, 2020, 70(1): 7-30. DOI:10.3322/caac.21590. [2] NAGTEGAAL I D, ODZE R D, KLIMSTRA D, et al. The 2019 WHO classification of tumours of the digestive system[J/OL]. Histopathology, 2020, 76(2): 182-188. DOI:10.1111/his.13975. [3] LI D, LIU L, FEVRIER H B, et al. Increased Risk of Colorectal Cancer

Identifiers

NCT: NCT07678788 · 34435353

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗