Study Evaluating Enbrel (Etanercept) in Patients With Ankylosing Spondylitis

NCT00227227

Last updated date
Study Location
Berlin, , 10719, Germany
Contact
1-800-718-1021

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Eligibility Criteria
condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Ankylosing Spondylitis
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

- Diagnosis of ankylosing spondylitis

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


- Contraindications according SmPC

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Advanced Information
Descriptive Information
Brief Title Study Evaluating Enbrel (Etanercept) in Patients With Ankylosing Spondylitis
Official Title Observational Study With Enbrel (Etanercept) in Patients With Ankylosing Spondylitis
Brief Summary The purpose of this study is to investigate the incidence of adverse events for patients with AS treated with Enbrel in usual care settings.
Detailed Description Not Provided
Study Type Observational
Study Design Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Not Provided
Study Population Not Provided
Condition Ankylosing Spondylitis
Intervention Not Provided
Study Groups/Cohorts Not 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 Status Completed
Estimated Enrollment
 (submitted: September 22, 2005)
750
Original Enrollment Same as current
Actual Study Completion Date June 2007
Primary Completion Date Not Provided
Eligibility Criteria

Inclusion Criteria:

  • Diagnosis of ankylosing spondylitis

Exclusion Criteria:

  • Contraindications according SmPC
Sex/Gender
Sexes Eligible for Study:All
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 Germany
Removed Location Countries  
 
Administrative Information
NCT Number NCT00227227
Other Study ID Numbers 101540
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Not Provided
Study Sponsor Wyeth is now a wholly owned subsidiary of Pfizer
Collaborators Not Provided
Investigators
Study Director:Medical MonitorWyeth is now a wholly owned subsidiary of Pfizer
Principal Investigator:Trial Manager[email protected]
PRS Account Wyeth is now a wholly owned subsidiary of Pfizer
Verification Date December 2007