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Study Comparing the Efficacy of Two Ibuprofen Formulations

Last updated on December 15, 2017

FOR MORE INFORMATION
Study Location
Salt Lake City, Utah, 84124 United States
Contact
1-800-718-1021
Eligibility criteria
Condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Pain
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
16-40 years
Inclusion criteria
The factors, or reasons, that allow a person to participate in a clinical study.
Show details

- 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 criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
Show details

- 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.

NCT00740857
Pfizer
Completed
Study Comparing the Efficacy of Two Ibuprofen Formulations

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Study Comparing the Efficacy of Two Ibuprofen Formulations
A Study Comparing the Efficacy of Two Ibuprofen Formulations
This is a study of healthy volunteers to compare how quickly different ibuprofen products relieve dental pain.
Not Provided
Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Pain
  • Drug: placebo
    2 placebo gels capsules delivered as a single dose.
  • Drug: ibuprofen Formulation 1
    2 marketed ibuprofen gels
  • Drug: ibuprofen Formulation 2
    2 marketed ibuprofen gels
  • Placebo Comparator: 1
    Intervention: Drug: placebo
  • Active Comparator: 2
    Intervention: Drug: ibuprofen Formulation 1
  • Active Comparator: 3
    Intervention: Drug: ibuprofen Formulation 2
Not Provided


*   Includes publications given by the data provider as well as publications
identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
211
November 2008
November 2008   (Final data collection date for primary outcome measure)

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.
Sexes Eligible for Study: All
16 Years to 40 Years   (Child, Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00740857
PV-08-24
No
Not Provided
Not Provided
Wyeth (Registry Contact: Clinical Trial Registry Specialist), Wyeth
Wyeth is now a wholly owned subsidiary of Pfizer
Not Provided
Study Director: Medical Monitor Wyeth is now a wholly owned subsidiary of Pfizer
Wyeth is now a wholly owned subsidiary of Pfizer
June 2011

ICMJE     Data element required by the

International Committee of Medical Journal Editors
and the
World Health Organization ICTRP

FOR MORE INFORMATION

Contact a representative by phone, email, or visiting thte study website. To get updates and notications about this trail, sign up using the form below.

BY PHONE

Pfizer Clinical Trials Contact Center

1-800-718-1021

BY EMAIL

Contact

[email protected]



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