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Study Evaluating Workload, Clinical and Therapeutic Management of Psoriatic Arthritis

Last updated on October 19, 2019

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

1. patients older than 18 years with a psoriatic arthritis diagnosis that go to
dermatologic and/or rheumatologic centers or primary care centers.

2. patients that receive pharmacologic treatment for their condition

3. patients that give their written consent to participate

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

1. patients older than 18 years with a psoriatic arthritis diagnosis that go to
dermatologic and/or rheumatologic centers or primary care centers.

2. patients that receive pharmacologic treatment for their condition

3. patients that give their written consent to participate

NCT00580632
Pfizer
Completed
Study Evaluating Workload, Clinical and Therapeutic Management of Psoriatic Arthritis

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Questions about a trial? Call or email to reach a Pfizer Clinical Trial Contact Center Representative

Pfizer Clinical Trials Contact Center

1-800-718-1021

[email protected]

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Descriptive Information
Brief TitleStudy Evaluating Workload, Clinical and Therapeutic Management of Psoriatic Arthritis
Official TitleWorkload, Clinical and Therapeutic Management of Psoriatic Arthritis
Brief SummaryIn Spain, there is little data available concerning the evolution and treatment of Psoriatic Arthritis by rheumatologists and dermatologists. This study is designed to obtain more data about the clinical and therapeutic management of Psoriatic Arthritis in Dermatology and Rheumatology Medical centers.
Detailed DescriptionNot Provided
Study TypeObservational
Study DesignObservational Model: Case-Only
Time Perspective: Retrospective
Target Follow-Up DurationNot Provided
BiospecimenNot Provided
Sampling MethodProbability Sample
Study PopulationPsoriatic Arthritis Patients with a representative geographic sample
ConditionPsoriatic 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
Actual Enrollment
 (submitted: December 26, 2007)
300
Original Actual EnrollmentSame as current
Actual Study Completion DateSeptember 2007
Actual Primary Completion DateSeptember 2007   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  1. patients older than 18 years with a psoriatic arthritis diagnosis that go to dermatologic and/or rheumatologic centers or primary care centers.
  2. patients that receive pharmacologic treatment for their condition
  3. patients that give their written consent to participate
Sex/Gender
Sexes Eligible for Study:All
Ages19 Years and older   (Adult, Older Adult)
Accepts Healthy VolunteersNo
ContactsContact information is only displayed when the study is recruiting subjects
Listed Location CountriesNot Provided
Removed Location Countries  
 
Administrative Information
NCT NumberNCT00580632
Other Study ID Numbers0881A-102389
Has Data Monitoring CommitteeNo
U.S. FDA-regulated ProductNot Provided
IPD Sharing StatementNot Provided
Responsible PartyWyeth (Registry Contact: Clinical Trials Registry Specialist), Wyeth
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
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]

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