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Clinical Trial Summary

The purpose of this research is to determine the proportion of women who achieve permanent cessation of bleeding after Uterine Balloon Therapy (UBT) for the treatment of heavy uterine bleeding.


Clinical Trial Description

This study was also designed to determine the effect of a post procedure curettage on bleeding patterns and post-operative discharge and pain. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00215618
Study type Interventional
Source Ethicon, Inc.
Contact
Status Completed
Phase Phase 3
Start date March 2003
Completion date September 2008

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