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Clinical Trial Summary

The investigators hypothesize that the combination of eflornithine and sulindac will be effective in reducing a three-year event rate of adenomas and second primary colorectal cancers in patients previously treated for Stages 0 through III colon or rectal cancer.


Clinical Trial Description

The purpose of this study is to assess whether the combination of eflornithine 500 mg and sulindac 150 mg (compared to corresponding placebos) has efficacy against colorectal lesions with respect to high-grade dysplasia, adenomas with villous features, adenomas 1 cm or greater, multiple adenomas, any adenomas >/= 0.3 cm, total advanced colorectal events, or total colorectal events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01349881
Study type Interventional
Source SWOG Cancer Research Network
Contact
Status Active, not recruiting
Phase Phase 3
Start date August 23, 2013
Completion date February 1, 2032

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