drugset
drugset / Trial / NCT03545893

Overnight Pain Treatment Investigating Opioids vs. Nonopioids

NCT03545893 ↗

Phase 4 Completed 70 enrolled University of Pennsylvania
RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2018-06-19
Primary completion
2019-02-07
Completion
2019-02-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ibuprofen Small molecule 600 mg —
Comparator Oxycodone Other / unclassified 5 mg Oral

Indications

No indication recorded.