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Study of MK0663/Etoricoxib in Postorthopedic Knee Replacement Surgery Pain
This study is not yet open for participant recruitment.
Verified by Merck, January 2009
Sponsored by: Merck
Information provided by: Merck
ClinicalTrials.gov Identifier: NCT00820027
  Purpose

The purpose of this study is to evaluate the efficacy and safety of etoricoxib compared to placebo and other pain medications in the treatment of postoperative pain.


Condition Intervention Phase
Postorthopedic Knee Replacement Surgery Pain
Drug: Comparator: etoricoxib (MK0663)
Drug: Comparator: ibuprofen
Drug: Comparator: placebo
Phase III

MedlinePlus related topics: Knee Replacement
Drug Information available for: Ibuprofen Dexibuprofen Etoricoxib
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Phase III Randomized, Double-Blind, Placebo- and Active-Comparator-Controlled, Multiple-Dose, Clinical Trial to Study the Safety and Efficacy of MK0663/Etoricoxib and Ibuprofen in the Treatment of Postorthopedic Knee Replacement Surgery Pain

Further study details as provided by Merck:

Primary Outcome Measures:
  • Overall analgesic effect as measured by pain intensity difference at rest over days 1 through 3 compare to placebo; Use of average total daily dose of morphine over days 1 through 3 compare to placebo; Safety and tolerability of etoricoxib over 7 days [ Time Frame: Days 1-3 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Overall analgesic effect as measured by pain intensity difference at rest over days 1 through 3 compare to ibuprofen [ Time Frame: Days 1-3 ] [ Designated as safety issue: No ]

Estimated Enrollment: 713
Study Start Date: January 2009
Estimated Study Completion Date: December 2009
Estimated Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Etoricoxib
Drug: Comparator: etoricoxib (MK0663)
Patients will receive either 120 mg or 90 mg etoricoxib tablets once daily and placebo to ibuprofen three times daily for 1 week following knee replacement surgery.
2: Experimental
Etoricoxib
Drug: Comparator: etoricoxib (MK0663)
Patients will receive either 120 mg or 90 mg etoricoxib tablets once daily and placebo to ibuprofen three times daily for 1 week following knee replacement surgery.
3: Active Comparator
Ibuprofen
Drug: Comparator: ibuprofen
Patients will receive 600 mg ibuprofen tablets three times daily and placebo to etoricoxib 60 mg and 90 mg once daily for 1 week following knee replacement surgery.
4: Placebo Comparator
Placebo
Drug: Comparator: placebo
Patients will receive placebo tablets three times daily for 1 week following knee replacement surgery.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients is 18 years of age or older
  • Patient is in generally good health and is scheduled to have a total knee replacement

Exclusion Criteria:

  • Patient is allergic, intolerant to, or has a history of a significant clinical or laboratory adverse experience associated with etoricoxib or other COX-2 inhibitors/NSAIDs, ibuprofen, morphine, or oxycodone, or has hypersensitivity to aspirin, or other NSAIDs
  • Patient has uncontrolled hypertension
  • Patient is currently a user of any illicit drugs, or has a history of drug or alcohol abuse within the past 5 years
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00820027

Contacts
Contact: Toll Free Number 1-888-577-8839

Sponsors and Collaborators
Merck
Investigators
Study Director: Medical Monitor Merck
  More Information

Responsible Party: Merck & Co., Inc. ( Executive Vice President, Clinical and Quantitative Sciences )
Study ID Numbers: 2009_502, MK0663-098
Study First Received: January 7, 2009
Last Updated: January 7, 2009
ClinicalTrials.gov Identifier: NCT00820027  
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Ibuprofen
Etoricoxib
Pain

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Cyclooxygenase Inhibitors
Enzyme Inhibitors
Pharmacologic Actions
Analgesics, Non-Narcotic
Sensory System Agents
Therapeutic Uses
Anti-Inflammatory Agents, Non-Steroidal
Analgesics
Peripheral Nervous System Agents
Antirheumatic Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on January 16, 2009