Clinical Trials Directory

Trials / Completed

CompletedNCT02101476

An Open Label, Prospective Study of the Analgesic Efficacy of Oral Xartemis Compared to Generic Oxycodone/APAP( Acetaminophen) in the Treatment of Moderate to Severe Post Operative Pain.

A Randomized, Open Label,Prospective Study of the Analgesic Efficacy of Oral Xartemis Compared to Generic Oxycodone/APAP (Acetaminophen) in the Treatment of Moderate to Severe Post Operative Pain

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
114 (actual)
Sponsor
Lotus Clinical Research, LLC · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the analgesic efficacy of Xartemis 15mg/650mg by mouth every 12 hours for the management of acute moderate to severe post operative pain to generic Oxycodone/APAP(acetaminophen) (Percocet) 10mg/650mg by mouth every 6 hours.

Conditions

Interventions

TypeNameDescription
DRUGPercocet10mg/650mg
DRUGXartemis15mg/650mg

Timeline

Start date
2014-05-01
Primary completion
2014-08-01
Completion
2014-10-01
First posted
2014-04-02
Last updated
2018-04-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02101476. Inclusion in this directory is not an endorsement.

An Open Label, Prospective Study of the Analgesic Efficacy of Oral Xartemis Compared to Generic Oxycodone/APAP( Acetamin (NCT02101476) · Clinical Trials Directory