A Study to Evaluate the Efficacy of MK0719 in the Prevention of Postoperative Dental Pain (0719-002)
Phase 2
Terminated
- Conditions
- Pain, Postoperative
- Registration Number
- NCT00424424
- Lead Sponsor
- Merck Sharp & Dohme LLC
- Brief Summary
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).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Male
- Target Recruitment
- 81
Inclusion Criteria
Not provided
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Exclusion Criteria
Not provided
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Proprietary Information - Exploratory (Non-Confirmatory) Trial
- Secondary Outcome Measures
Name Time Method Proprietary Information - Exploratory (Non-Confirmatory) Trial