Clinical Trials Directory

Trials / Terminated

TerminatedNCT01900795

An Analgesic Study to of V117957 for the Treatment of Postsurgical Pain Due to Third Molar Extraction

A Phase 2a, Single-Center, Randomized, Double-Blind, Double- Dummy, Placebo- and Active-Controlled Analgesic Study of an Oral Dose of V117957 4.5 mg for the Treatment of Postsurgical Pain Due to Third Molar Extraction

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
114 (actual)
Sponsor
Purdue Pharma LP · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to assess the analgesic properties of an oral dose of V117957 4.5 mg aqueous suspension in the third molar extraction model

Conditions

Interventions

TypeNameDescription
DRUGV117957V117957 4.5 mg suspension taken orally after surgery.
DRUGIbuprofenIbuprofen 400 mg tablets taken orally after surgery.
DRUGPlaceboPlacebo taken orally after surgery.

Timeline

Start date
2013-07-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2013-07-16
Last updated
2013-12-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01900795. Inclusion in this directory is not an endorsement.