Study Comparing the Efficacy of Two Ibuprofen Formulations
Completed · Phase 4 · Has a placebo group
Conditions studied: Pain
In brief
This is a study of healthy volunteers to compare how quickly different ibuprofen products relieve dental pain.
Key facts
- Study ID
- NCT00740857
- Run by
- Wyeth is now a wholly owned subsidiary of Pfizer
- People needed
- 211
- Starts
- 2008-08-01
- Expected to finish
- 2008-11-01
- Last updated by the study team
- 2011-06-06
Who can join
Age: 16 and older, up to 40. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 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.
Where it is running
- Study site — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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