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)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (1 locations)

    1

    Salt Lake City, Utah, United States, 84124