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Clinical Trial Summary

The purpose of this study is to compare maximum pain scores between patients seeking induced abortion and requiring cervical preparation with osmotic dilators. Patients will be randomized to receive prescription for ibuprofen alone or to receive prescription for ibuprofen + oxycodone for overnight pain management after cervical preparation with osmotic dilators. Data collected in-person and through a text-messaging platform.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03545893
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase Phase 4
Start date June 19, 2018
Completion date February 7, 2019