Expired Study
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Austin, Texas 78705


Purpose:

The study hypothesis is that single and multiple doses of ibuprofen 600 mg ER caplets provide analgesic efficacy superior to placebo over 12-hour dosing intervals.


Criteria:

Inclusion Criteria: - Males and females 16 to 40 years of age - Subjects who undergo surgical removal of at least two third molars - One of which must be a partial or full bony mandibular impaction - Subjects must have at least moderate baseline pain (a score of 2 on the categorical pain severity rating scale) confirmed by a score of at least 50 mm on the 100-mm visual analog scale-pain severity rating scale (VAS-PSR) Exclusion Criteria: - Acute localized dental infection at the time of surgery that could confound the post-surgical evaluation - Presence or history of any significant organ disease - Use of prescription or OTC first generation antihistamines - Females who are pregnant, lactating or of childbearing potential and not using a medically approved method to prevent pregnancy


NCT ID:

NCT01266161


Primary Contact:

Study Director
Pfizer CT.gov Call Center
Pfizer


Backup Contact:

N/A


Location Contact:

Austin, Texas 78705
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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