Study Evaluating Anxiety and Depression in Patients With Psoriatic Arthritis
NCT00884468
ABOUT THIS STUDY
FOR MORE INFORMATION
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1-800-718-1021
- Patients both genders over 18 years old
- Patients with PsA diagnosis
- Patients with PsA that suffer from other rheumatologic diseases or non-concomitant
rheumatologic diseases that the investigator considers not to be appropriate for the
study.
- Patients with any medical or physical condition (cognitive damage or difficulties for
understanding) that create difficulties for reading and completing the questionnaires
described in the protocol.
- Patients that in the study period are taking part in another clinical trial.
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Descriptive Information | ||||
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Brief Title | Study Evaluating Anxiety and Depression in Patients With Psoriatic Arthritis | |||
Official Title | Anxiety and Depression in Patients With Psoriatic Arthritis: Prevalence and Characteristics | |||
Brief Summary | This is an epidemiological non-interventional study assessing the prevalence of anxiety and/or depression disorders in patients suffering from Psoriatic Arthritis (PsA) in Spain. | |||
Detailed Description | Not Provided | |||
Study Type | Observational | |||
Study Design | Observational Model: Cohort Time Perspective: Cross-Sectional | |||
Target Follow-Up Duration | Not Provided | |||
Biospecimen | Not Provided | |||
Sampling Method | Probability Sample | |||
Study Population | Patients with PsA from outpatient's surgery or primary health care centres | |||
Condition | Psoriatic Arthritis | |||
Intervention | Not Provided | |||
Study Groups/Cohorts | 1
Patients with PsA that fulfill the eligibility criteria of the study | |||
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 Status | Completed | |||
Actual Enrollment | 384 | |||
Original Actual Enrollment | Same as current | |||
Actual Study Completion Date | December 2008 | |||
Actual Primary Completion Date | December 2008 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria | Inclusion criteria:
Exclusion criteria:
| |||
Sex/Gender |
| |||
Ages | 18 Years and older (Adult, Older Adult) | |||
Accepts Healthy Volunteers | No | |||
Contacts | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries | Spain | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number | NCT00884468 | |||
Other Study ID Numbers | 0881A5-4468 | |||
Has Data Monitoring Committee | No | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement | Not Provided | |||
Responsible Party | Wyeth (Registry Contact: Clinical Trial Registry Specialist), Wyeth | |||
Study Sponsor | Wyeth is now a wholly owned subsidiary of Pfizer | |||
Collaborators | Not Provided | |||
Investigators |
| |||
PRS Account | Wyeth is now a wholly owned subsidiary of Pfizer | |||
Verification Date | May 2009 |