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
| Type | Name | Description |
|---|---|---|
| DRUG | Percocet | 10mg/650mg |
| DRUG | Xartemis | 15mg/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.