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Clinical Trial Summary

Our primary objective will be to determine if a strong opioid, oxycodone, given at a dose recommended for severe pain in addition to ibuprofen decreases maximum pain scores compared to ibuprofen and placebo in women undergoing medical abortion (MAB). Results of this study will help future providers understand whether prescribing opioids are an important adjunct for pain control in women undergoing MAB.


Clinical Trial Description

This study will include 152 women undergoing MAB. Women will be randomized to oxycodone 10mg oral versus placebo and stratified by gestational age (<7wks, 7-10wks). The primary outcome will be maximum reported pain score measured at 6-8 hours and 24 hours after misoprostol administration. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03139240
Study type Interventional
Source Oregon Health and Science University
Contact
Status Completed
Phase Phase 4
Start date May 1, 2017
Completion date May 31, 2018

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