Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01350622

Efficacy of PENNSAID® for Pain Management in the Emergency Department

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of Utah · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGPENNSAIDactive treatment with PENNSAID and oral placebo. Subjects will apply 40 drops of Pennsaid to the affected ankle joint once, and will take a single placebo pill.
DRUGDiclofenac hydroxyethylpyrrolidineactive treatment oral Diclofenac and PENNSAID placebo. Patients will take a single 50mg dose of oral diclofenac and will apply 40 drops of placebo lotion (2.3% DMSO) to the affected ankle once.

Timeline

Start date
2011-12-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2011-05-10
Last updated
2016-12-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01350622. Inclusion in this directory is not an endorsement.