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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06416501
Other study ID # FudanUcf
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 11, 2024
Est. completion date June 15, 2024

Study information

Verified date May 2024
Source Fudan University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to investigate the pathological characteristics and surgical outcomes of stage III CRC patients detected through screening. Data extracted from the database included the following patient information: age at diagnosis, gender, tumor location, neoadjuvant therapy, surgical procedures, histologic type, differentiation, vascular invasion, perineural invasion, pathological T stage, pathological N stage, and survival outcomes.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 4000
Est. completion date June 15, 2024
Est. primary completion date June 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Patients who underwent radical surgery for CRC, had confirmed stage III CRC through postoperative pathology, had no prior history of cancer before surgery, and had clear cancer detection information.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mode of detection
Mode of detection

Locations

Country Name City State
China Xinxiang Li Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Fudan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary overall survival The duration from the initial treatment to either death from any cause or the last recorded follow-up, whichever came first.
Assessed up to 100 months.
the duration from the initial treatment to either death from any cause or the last recorded follow-up, whichever came first. Assessed up to 100 months.
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