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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ChiCTR
Last refreshed on: 11 September 2017
Main ID:  ChiCTR-IOR-17012626
Date of registration: 2017-09-09
Prospective Registration: Yes
Primary sponsor: Fudan University Zhongshan Hospital
Public title: Effect and Safety Evaluation of anti-EGFR therapy combined local therapy for unresectable colonrectal cancer Chinese Patients
Scientific title: Effect and Safety Evaluation of anti-EGFR therapy combined local therapy for unresectable colonrectal cancer Chinese Patients
Date of first enrolment: 2017-09-18
Target sample size: Intervention Group:120;Control Group:60;
Recruitment status: Recruiting
URL:  http://www.chictr.org.cn/showproj.aspx?proj=21313
Study type:  Interventional study
Study design:  Randomized parallel controlled trial  
Phase:  Other
Countries of recruitment
China
Contacts
Name: Zhou Bo   
Address:  180 Fenglin Road, Shanghai, China 200032
Telephone: +86 13621604953
Email: zhou.bo@zs-hospital.sh.cn
Affiliation:  Fudan University Zhongshan Hospital
Name: Zhou Bo   
Address:  180 Fenglin Road, Shanghai, China 200032
Telephone: +86 13621604953
Email: zhou.bo@zs-hospital.sh.cn
Affiliation:  Fudan University Zhongshan Hospital
Key inclusion & exclusion criteria
Inclusion criteria: 1. Patients with colonrectal cancer liver metastasis, and RAS wild type;
2. No jaundice obstructive;
3. Patients are willing to take cetuximab;
4. Patients are willing to join the research, to accept the informed consent, to privide specimen;
5. Aged above 18 years and lower than 80 years;
6. The lesion can be measured.

Exclusion criteria: 1. Patients who can be followed.
2. Patients who have no ability to determination
3. Patients are taking other targeted therapy.
4. Patients with severe organ funtion disorders.
5. Survival time lower than 3 months
6. Intolerant or allergic to cetuximab
7. Contraindications for cetuximab


Age minimum: 18
Age maximum: 80
Gender: Both
Health Condition(s) or Problem(s) studied
colonrectal cancer liver metastasis
Intervention(s)
Intervention Group:chemotherapy and target therapy combined TACE;Control Group:chemotherapy and target therapy;
Primary Outcome(s)
Image Evaluation;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Fund by Chinese Society of Clinical Oncology, CSCO
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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