Registry of Etanercept Use in Patients With Rheumatoid Arthritis in Clinical Practice in Taiwan
NCT00888576
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| Descriptive Information | ||||
|---|---|---|---|---|
| Brief Title | Registry of Etanercept Use in Patients With Rheumatoid Arthritis in Clinical Practice in Taiwan | |||
| Official Title | A Registry Study to Describe the Implications of Therapeutic Management of Etanercept in Patients With Rheumatoid Arthritis | |||
| Brief Summary | The purpose of this study is to develop a registry with safety and efficacy data on the use of etanercept in clinical practice in Taiwan. | |||
| Detailed Description | Not Provided | |||
| Study Type | Observational | |||
| Study Design | Observational Model: Cohort Time Perspective: Prospective | |||
| Target Follow-Up Duration | Not Provided | |||
| Biospecimen | Not Provided | |||
| Sampling Method | Non-Probability Sample | |||
| Study Population | clinic | |||
| Condition | Rheumatoid Arthritis | |||
| Intervention | Not Provided | |||
| Study Groups/Cohorts | 1
Non-intervention | |||
| 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 | 441 | |||
| Original Estimated Enrollment | 500 | |||
| Actual Study Completion Date | December 2011 | |||
| Actual Primary Completion Date | December 2011 (Final data collection date for primary outcome measure) | |||
| Eligibility Criteria | Inclusion Criteria: Main Inclusion Criteria: 1) Male or female patients aged > 20 years; 2) Patients who have already been selected and approved under the Taiwan National Health Insurance Program to receive 24 weeks of etanercept for rheumatoid arthritis. Main Exclusion Criteria: Exclusion Criteria: None | |||
| Sex/Gender |
| |||
| Ages | 20 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 | Taiwan | |||
| Removed Location Countries | ||||
| Administrative Information | ||||
| NCT Number | NCT00888576 | |||
| Other Study ID Numbers | 0881A1-4445 | |||
| Has Data Monitoring Committee | No | |||
| U.S. FDA-regulated Product | Not Provided | |||
| IPD Sharing Statement | Not Provided | |||
| Responsible Party | Pfizer | |||
| Study Sponsor | Pfizer | |||
| Collaborators | Not Provided | |||
| Investigators |
| |||
| PRS Account | Pfizer | |||
| Verification Date | February 2012 | |||