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Clinical Trial Summary

This study sets up the final study end point and three detailed goals as the following. The main objective of study: This trial is done to assess the safety and benefit of early adjuvant chemotherapy from 10 to 14 days after surgery compared with conventional commencement after 2weeks for treatment of patients with colon cancer. Detailed goal of study: The primary endpoint: This study is designed to assess whether early commencement of adjuvant chemotherapy improves the 3-year disease-free survival, overall survival and recurrence rate. The secondary endpoint: This study aims to compare short-term cumulative complications between early and conventional commencement of adjuvant chemotherapy after laparoscopic resection of colon cancer. This study will also assess the quality of life and side effects of chemotherapy.


Clinical Trial Description

Chemotherapy regimen: FOLFOX-6, every 2weeks, total 12 cycles treatment - day1: Oxaliplatin 85mg/m2 - day1: Leucovorin 200mg/m2 - day1: 5-FU 400mg/m2 IV bolus - 2,400mg/m2 over 46 hours ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01460589
Study type Interventional
Source Kyungpook National University Hospital
Contact
Status Active, not recruiting
Phase Phase 3
Start date November 2011
Completion date December 2024

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