Status:
COMPLETED
A Study to Asses the Effect of MK0663 in the Treatment of Patients With Postoperative Dental Pain (0663-092)
Lead Sponsor:
Organon and Co
Conditions:
Postoperative Dental Pain
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
The purpose of this study is to compare the pain relieving effect of different doses of MK0663 with placebo and other pain relievers/analgesics in patients with postoperative dental pain. Pain intensi...
Eligibility Criteria
Inclusion
- Patients must be scheduled to have 2 or more third molars removed, at least 1 of which is partially embedded in bone and is impacted in the lower jaw
- Patients must be experiencing moderate to severe pain following the dental procedure
Exclusion
- Previous molar extraction within the past 45 days
- Personal or family history of an inherited bleeding disorder
- Uncontrolled high blood pressure
Key Trial Info
Start Date :
June 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2009
Estimated Enrollment :
588 Patients enrolled
Trial Details
Trial ID
NCT00694369
Start Date
June 1 2008
End Date
January 1 2009
Last Update
February 9 2022
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