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Study Evaluating Health Related Utility in Rheumatoid Arthritis

Last updated on November 15, 2019

FOR MORE INFORMATION
Study Location
Darlinghurst, New South Wales, 2010 Australia
Contact
1-800-718-1021
Eligibility criteria
Condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Rheumatoid Arthritis
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18 + years
Inclusion criteria
The factors, or reasons, that allow a person to participate in a clinical study.
Show details

- Male or female patient with clinically defined rheumatoid arthritis diagnosed for at
least 3 months

- Age 18 years or older

- Ability to complete the study documents in English

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

· Current participation in a blinded trial of an investigational treatment

NCT00471874
Pfizer
Completed
Study Evaluating Health Related Utility in Rheumatoid Arthritis

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Pfizer Clinical Trials Contact Center

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[email protected]

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Descriptive Information
Brief TitleStudy Evaluating Health Related Utility in Rheumatoid Arthritis
Official TitleAn Observational Study to Examine the Relationship Between Rheumatoid Arthritis Disease Severity and Health Related Utility
Brief SummaryThe purpose of this study is to determine in Australia what effect rheumatoid arthritis has on quality of life, and also to determine the costs that are associated with having rheumatoid arthritis.
Detailed Description

At a routine visit to the clinic, patients will be asked to answer questions about their symptoms, have a routine examination by the doctor, fill out a questionnaire that will ask questions about them, about their arthritis, about how it affects their well being and quality of life, and about treatment and costs. The questionnaire will take them about 30 minutes to complete. A blood test may also be required.

This ends the patient's involvement with the study.

Study TypeObservational
Study DesignTime Perspective: Retrospective
Target Follow-Up DurationNot Provided
BiospecimenNot Provided
Sampling MethodNot Provided
Study PopulationNot Provided
ConditionRheumatoid Arthritis
InterventionNot Provided
Study Groups/CohortsNot Provided
Publications *Not Provided


*   Includes publications given by the data provider as well as publications
identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment StatusCompleted
Estimated Enrollment
 (submitted: May 9, 2007)
250
Original Estimated EnrollmentSame as current
Actual Study Completion DateDecember 2007
Primary Completion DateNot Provided
Eligibility Criteria

Inclusion Criteria:

  • Male or female patient with clinically defined rheumatoid arthritis diagnosed for at least 3 months
  • Age 18 years or older
  • Ability to complete the study documents in English

Exclusion Criteria:

· Current participation in a blinded trial of an investigational treatment

Sex/Gender
Sexes Eligible for Study:All
Ages18 Years and older   (Adult, Older Adult)
Accepts Healthy VolunteersNo
ContactsContact information is only displayed when the study is recruiting subjects
Listed Location CountriesAustralia
Removed Location Countries  
 
Administrative Information
NCT NumberNCT00471874
Other Study ID Numbers0881X1-4427
Has Data Monitoring CommitteeNo
U.S. FDA-regulated ProductNot Provided
IPD Sharing StatementNot Provided
Responsible PartyNot Provided
Study SponsorWyeth is now a wholly owned subsidiary of Pfizer
CollaboratorsNot Provided
Investigators
Study Director:Medical MonitorWyeth is now a wholly owned subsidiary of Pfizer
Principal Investigator:Trial ManagerFor Australia, [email protected]
PRS AccountWyeth is now a wholly owned subsidiary of Pfizer
Verification DateDecember 2007

FOR MORE INFORMATION

Contact a representative by phone, email, or visiting the study website. Please see the references below:

BY PHONE

Pfizer Clinical Trials Contact Center

1-800-718-1021

BY EMAIL

Contact

[email protected]

Call Now