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Clinical Trial Summary

This study will evaluate the impact of low dose aspirin on normal fallopian tube fimbriae in women who have surgery to have their fallopian tubes removed. Participants will take a low dose of aspirin for 2 weeks before their surgery. A portion of the removed fallopian tubes will also be collected for future research and routine pathology purposes.


Clinical Trial Description

Subjects in this study will receive low dose aspirin for 14 days before undergoing surgery to remove fallopian tubes removed to determine whether aspirin decreases inflammation in the fallopian tube. Subjects will also submit blood samples at their initial visit with their oncologist, at the time of surgery and at the pre-operative visit to measure inflammation markers and blood counts. A portion of the subject's fallopian tube will be collected for future research studies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03771651
Study type Interventional
Source University of Oklahoma
Contact
Status Active, not recruiting
Phase Early Phase 1
Start date March 1, 2019
Completion date June 2025

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