A Study to Evaluate the Efficacy of MK0719 in the Prevention of Postoperative Dental Pain
This study is being conducted to evaluate the safety and tolerability of the drug and to evaluate its efficacy compared to placebo and to ibuprofen in the prevention of postoperative dental pain in male patients.
This is an early phase trial and some specific protocol information is proprietary and not publicly available at this time. (Full information is available to trial participants).
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Primary Purpose: Prevention
|Official Title:||Proprietary Information - Exploratory (Non-Confirmatory) Trial|
Please refer to this study by its ClinicalTrials.gov identifier: NCT00424424
|Study Director:||Medical Monitor||Merck Sharp & Dohme Corp.|