Status:
COMPLETED
Study Comparing the Efficacy of Two Ibuprofen Formulations
Lead Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Conditions:
Pain
Eligibility:
All Genders
16-40 years
Phase:
PHASE4
Brief Summary
This is a study of healthy volunteers to compare how quickly different ibuprofen products relieve dental pain.
Eligibility Criteria
Inclusion
- Inclusion criteria :
- Outpatients with post-operative pain following surgical extraction of third molars,
- examined by the attending dentist or physician and medically cleared to participate in the study,
- in general good health and have no contraindications to the study or rescue medication.
- Exclusions criteria:
- any serious medical condition,
- acute localized dental infection at the time of surgery ,
- females who are pregnant, lactating, of child-bearing potential, or post-menopausal for less than 2 years and not using a medically approved method of contraception.
Exclusion
Key Trial Info
Start Date :
August 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2008
Estimated Enrollment :
211 Patients enrolled
Trial Details
Trial ID
NCT00740857
Start Date
August 1 2008
End Date
November 1 2008
Last Update
June 6 2011
Active Locations (1)
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1
Salt Lake City, Utah, United States, 84124