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MK0686 in Postsurgery Dental Pain (0686-002)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00533403
First Posted: September 21, 2007
Last Update Posted: June 26, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Merck Sharp & Dohme Corp.
September 19, 2007
September 21, 2007
June 26, 2015
July 2004
November 2004   (Final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00533403 on ClinicalTrials.gov Archive Site
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MK0686 in Postsurgery Dental Pain (0686-002)
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To compare the pain relieving effect of MK0686 to placebo or ibuprofen after dental surgery.
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Interventional
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Pain, Postoperative
Drug: MK0686
Not Provided
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
114
November 2004
November 2004   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Men and women ages 18-45 years who are scheduled to have 2 or more third molars (wisdom teeth) removed
  • Patients must agree to remain in the clinic for 24 hours after surgery

Exclusion Criteria:

  • Patient has history of heart disease, asthma, pulmonary disease
  • Patient must discontinue use of certain pain medicines 24-72 hours prior to the surgery
Sexes Eligible for Study: All
18 Years to 45 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
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NCT00533403
0686-002
2007_617
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Merck Sharp & Dohme Corp.
Merck Sharp & Dohme Corp.
Not Provided
Study Director: Medical Monitor Merck Sharp & Dohme Corp.
Merck Sharp & Dohme Corp.
June 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP