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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03958435
Other study ID # REDUCE201809
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 9, 2018
Est. completion date December 15, 2023

Study information

Verified date May 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Ying Yuan, Ph.D&MD
Phone +86-571-87784795
Email yuanying1999@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background: 1. . The incidence and mortality of colon cancer are high in China and in the world. 2. . The treatment of many patients in the real world is not standardized, and there are problems such as over-treatment or under-treatment. To explore the adjuvant treatment of colon cancer in the Chinese population, this study will retrospectively analyze real-world data on adjuvant therapy for colon cancer in Chinese patients after radical surgery. The purpose of research: 1. . Current status of adjuvant therapy for stage II-III colon cancer in the real world: chemotherapy regimen, chemotherapy time, efficacy, safety, etc. 2. . Comparison of efficacy and safety of different adjuvant chemotherapy time (<3 months vs. >=3 months) in high-risk stage II and III colon cancer patients in the real world 3. . Comparison of efficacy and safety of different adjuvant chemotherapy regimens (XELOX vs. FOLFOX) in high-risk stage II and III colon cancer patients in the real world


Recruitment information / eligibility

Status Recruiting
Enrollment 20000
Est. completion date December 15, 2023
Est. primary completion date October 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients who are sick after January 2010 - Age is older than 18 - Surgical pathology confirmed TNM stage II-III (AJCC 7th edition) colon cancer Exclusion Criteria: - Combine other tumors - Pathological information is not clear - Researchers believe that other reasons are not suitable for enrollment

Study Design


Locations

Country Name City State
China SAHZU Hangzhou Zhejinag
China Jiangsu Province People Hospital Nanjing Jiangsu
China Changhai Hospital of Shanghai Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of patients with chemotherapy regimen for adjuvant therapy after stage II and stage III colon cancer Percentage of patients with chemotherapy regimen for adjuvant therapy after stage II and stage III colon cancer From patients after stage II and stage III colon cancer radical resection to until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 120 months.
Primary Percentage of patients with different chemotherapy time for adjuvant therapy for stage II and stage III colon cancer Percentage of patients with different chemotherapy time for adjuvant therapy for stage II and stage III colon cancer From patients after stage II and stage III colon cancer radical resection to until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 120 months.
Primary Percentage of Participants with treatment-related Adverse Events as Assessed by CTCAE v4.0 for adjuvant therapy for stage II and stage III colon cancer Percentage of Participants with treatment-related Adverse Events as Assessed by CTCAE v4.0 for adjuvant therapy for stage II and stage III colon cancer From patients after stage II and stage III colon cancer radical resection to until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 120 months.
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