Phase
Condition
Pain
Pain (Pediatric)
Chronic Pain
Treatment
N/AClinical Study ID
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Healthy, ambulatory, male and female volunteers ages 18-65 years old
History of an onset of tension type headaches before age 50
Experiencing over the last year ≥ 4 tension type headaches of at least moderateintensity per month and with the majority of headaches lasting greater than threehours, that meet commonly recognized criteria for diagnosis per the InternationalHeadache Society
History of response to treatment with over-the-counter (OTC) analgesics
Understand the pain rating scales (as judged by the trial coordinator)
Present with at least moderate headache pain on a 0-10 point numerical rating scale (ascore of at least 4 on an 11 point scale ranging from 0 to 10) at the Treatment Visit
Onset of pain within three hours of the Treatment Visit
Confirmation by a physician of acute tension type headache symptoms as described bythe International Headache Society diagnostic criteria
Exclusion
Exclusion Criteria:
History of hypersensitivity to aspirin, salicylates, other NSAIDs, acetaminophen, andsimilar pharmacological agents or components of the investigational products,including the placebo
Use of any immediate release analgesic/anti-pyretic within four hours or use of anysustained release or long acting analgesic/anti-pyretic within 12 hours proceedingadministration of Investigational Product
Presence of symptoms that are consistent with menstrual headache or migraine headacheas described by the International Headache Society diagnostic criteria
History of migraine headaches more than once per month
Relevant concomitant disease such as asthma (exercise induced asthma is permitted),chronic sinusitis or nasal structural abnormalities causing greater than 50 percentobstruction (polyposis nasi, marked septal deviation) that can interfere with theconduct of the trial in the judgment of the Investigator
Current or past history of bleeding disorder(s)
History of gastrointestinal bleeding or perforation, related to previous NonsteroidalAnti-inflammatory Drugs (NSAID) therapy. Active, or history of recurrent pepticulcer/hemorrhage (two or more distinct episodes of proven ulceration or bleeding)
Recent head or neck trauma (within 2 weeks)
Current use of blood thinning (anticoagulant), low dose aspirin, or steroid drug
Study Design
Connect with a study center
Westside Family Medical Center
Kalamazoo, Michigan 49009
United StatesSite Not Available
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