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Sponsored by: |
Merck |
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Information provided by: | Merck |
ClinicalTrials.gov Identifier: | NCT00533403 |
To compare the pain relieving effect of MK0686 to placebo or ibuprofen after dental surgery.
Condition | Intervention | Phase |
---|---|---|
Pain, Postoperative |
Drug: MK0686 |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study |
Ages Eligible for Study: | 18 Years to 45 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | 2007_617 |
Study First Received: | September 19, 2007 |
Last Updated: | September 19, 2007 |
ClinicalTrials.gov Identifier: | NCT00533403 |
Health Authority: | United States: Food and Drug Administration |
Signs and Symptoms Postoperative Complications Toothache Pain Pain, Postoperative |
Pathologic Processes |