Efficacy of a Single Dose of Aspirin vs. Acetaminophen in Tension Type Headache

Last updated: December 17, 2018
Sponsor: Bayer
Overall Status: Terminated

Phase

3

Condition

Pain

Pain (Pediatric)

Chronic Pain

Treatment

N/A

Clinical Study ID

NCT01552798
15771
  • Ages 18-65
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The purpose of this trial is to determine if a single, oral dose of a fast release aspirin 1000 mg provides relief compared to acetaminophen 1000 mg and placebo in subjects with tension-type headache pain.

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

Total Participants: 9
Study Start date:
March 12, 2012
Estimated Completion Date:
June 04, 2012

Connect with a study center

  • Westside Family Medical Center

    Kalamazoo, Michigan 49009
    United States

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.