Study of Etoricoxib for the Treatment of Muscle Pain and Inflammation Induced by Eccentric Exercise

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
X-pert Med GmbH
ClinicalTrials.gov Identifier:
NCT01271348
First received: January 5, 2011
Last updated: October 31, 2011
Last verified: October 2011

January 5, 2011
October 31, 2011
January 2011
October 2011   (final data collection date for primary outcome measure)
Pain during muscle contraction [ Time Frame: 7 days ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01271348 on ClinicalTrials.gov Archive Site
Not Provided
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Study of Etoricoxib for the Treatment of Muscle Pain and Inflammation Induced by Eccentric Exercise
Multiple-dose, Randomized, Double Blinded, Placebo-controlled, Cross Over Study of Etoricoxib for the Treatment of Muscle Pain and Inflammation Induced by Eccentric Exercise

Comparison of the effect of etoricoxib to placebo on muscle pain caused by eccentric contractions

Not Provided
Interventional
Phase 1
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Muscle Pain
  • Drug: Etoricoxib
    Etoricoxib film tablet, 90 mg, q.d.
  • Drug: placebo
    Placebo tablet, q.d.
  • Active Comparator: Etoricoxib
    Intervention: Drug: Etoricoxib
  • Placebo Comparator: Placebo tablet
    Intervention: Drug: placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
October 2011
October 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Signed and dated informed consent prior to participation
  • Subjects in good health as determined by the Investigator
  • Age 18-40 or 50-70
  • BMI > 20 and < 30
  • Pain in the target muscle (thigh) during muscle contraction of at least 5 on an 11 point categorical pain rating scale
  • Willing to abstain from any physical therapy, hard physical work, exercise or sauna during the study treatment periods (Screening to Final Visit)
  • For females, subjects of childbearing potential (including peri-menopausal women who have had a menstrual period within 1 year) must be using appropriate birth control (defined as a method which results in a low failure rate, i.e., less than 1% per year when used consistently and correctly, such as implants, injectables, some intrauterine contraceptive devices (IUDs), sexual abstinence, or a vasectomized partner). Oral contraceptive medications are not allowed in this study. Female subjects, who are surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy) are allowed for participation

Exclusion Criteria:

  • Participation in another clinical study within the last 30 days and during the study
  • Subjects who are inmates of psychiatric wards, prisons, or other state institutions
  • Investigator or any other team member involved directly or indirectly in the conduct of the clinical study
  • Pregnancy or lactation
  • Alcohol or drug abuse
  • Malignancy within the past 2 years with the exception of in situ removal of basal cell carcinoma
  • Known hypersensitivity to etoricoxib or other NSAID´s including Cox-2, or any of their excipients
  • Bronchospasm, acute rhinitis, nasal congestion, angioneurotic edema, urticaria or allergic reactions after taking aspirin or other NSAIDs including Cox-2 inhibitors
  • Major traumatic lesions (e.g. fracture, tendon or muscle ruptures) of the musculo-sceletal system of the lower limbs
  • Pain conditions which might interfere with pain rating during the study, e.g. neuropathic pain
  • Significant neurological or psychiatric symptoms resulting in disorientation, memory impairment, or inability to report accurately (e.g. depressive disorders, Alzheimer's disease, schizophrenia or other psychosis), that in the investigator's opinion may affect efficacy or safety assessments or may compromise subject safety during the study
  • Heart failure (NYHA II-IV)
  • Long term blood pressure > 140/90 mm Hg without adequate treatment
  • Peripheral arterial disease, coronary heart disease and/or cerebrovascular disease
  • History of stroke or myocardial infarction
  • Clinically relevant ECG changes
  • Estimated creatinine clearance < 60 ml/min
  • Liver dysfunction (e.g. defined by ALT and/or AST levels above upper limit of normal range)
  • Coagulopathy or bleeding diathesis, or concomitant use of anticoagulants including low dose aspirin
  • History of pancreatitis, peptic ulcers or gastrointestinal bleedings
  • Inflammatory GI disease (e.g. M. Crohn, colitis ulcerosa)
  • Any other analgesic therapy including cough and cold drugs containing analgesic properties as well as any other substance used for the treatment of pain during the study observation period (Screening to final Visit)
  • Any other drug that might alter pain perception like CNS active drugs
  • Statins within 3 months of screening and throughout the study
  • Oral anticonceptives
Both
18 Years to 70 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT01271348
XPM-032
Not Provided
X-pert Med GmbH
X-pert Med GmbH
Not Provided
Study Chair: Matthias Rother, M.D. Director Clinical Operations
X-pert Med GmbH
October 2011

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