drugset / Trial / NCT00291694

Protocol for Women at Increased Risk of Developing Breast Cancer

NCT00291694

RandomizedParallel-groupDouble-blindPrevention

Summary

To assess the effects of twelve months of celecoxib administration by evaluating breast tissue needle aspirations, to determine if cell growth can be slowed.

Timeline

Start
2003-04
Primary completion
2009-12
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Celecoxib Other / unclassified 400 mg Oral

Indications