Efficacy of PENNSAID® for Pain Management in the Emergency Department
Withdrawn before enrolling · Not applicable · Has a placebo group
Conditions studied: Pain, Ankle Sprain
In brief
The primary objective of this study is to compare the pain relieving effect and speed of onset of PENNSAID to that of standard oral diclofenac under double blind conditions using a growth curve approach to pain measurement. The investigators will test the hypothesis that PENNSAID will provide more rapid pain relief than oral diclofenac during the ED visit. The secondary goal of the proposed work is to discover and model the onset and course of pain relief during the emergency department (ED) visit.
Key facts
- Study ID
- NCT01350622
- Run by
- University of Utah
- People needed
- 0
- Starts
- 2011-12-01
- Expected to finish
- 2012-12-01
- Last updated by the study team
- 2016-12-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- University of Utah — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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