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Clinical Trial Summary

The aims of the trial are (1) to determine the tolerability rate in the setting of a multi-centre study and (2) to determine secondary tolerability endpoints, toxicity rates and complete pathologic response rate in patients with locally advanced rectal cancer who are treated with an integrated preoperative radiotherapy with FOLFOX chemotherapy regimen.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01013805
Study type Interventional
Source Trans-Tasman Radiation Oncology Group (TROG)
Contact
Status Completed
Phase Phase 2
Start date November 2009
Completion date December 2012

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