Study Evaluating Impact of the Use of a Computer-based Tool on the Clinical Management of RA Patients
NCT00895050
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Adult Trials: 18+ Years
Main
- Patients with other muscle skeletal, rheumatic and/or degenerative diseases different
from RA.
- Patients who are taking part or have taken part in a clinical trial or in a study with
drugs within the last 12 months. Any condition that, in the investigator's judgment
would interfere with the subject's ability to comply with protocol requirements or
give informed consent.
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| Descriptive Information | ||||
|---|---|---|---|---|
| Brief Title | Study Evaluating Impact of the Use of a Computer-based Tool on the Clinical Management of RA Patients | |||
| Official Title | Impact of the Use of a Computer-based Tools on the Clinical Management and Evolution of Patients With Rheumatoid Arthritis. | |||
| Brief Summary | The primary purpose of this study is to evaluate a computer-based tool on the clinical management of patients with rheumatoid arthritis in Spain. | |||
| 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 | Patients with RA treated in rheumatology offices | |||
| Condition | Rheumatoid Arthritis | |||
| Intervention | Other: Review of clinical records | |||
| Study Groups/Cohorts | 1
Patients diagnosed with RA Intervention: Other: Review of clinical records | |||
| 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 | 321 | |||
| Original Estimated Enrollment | 300 | |||
| Actual Study Completion Date | January 2011 | |||
| Actual Primary Completion Date | January 2011 (Final data collection date for primary outcome measure) | |||
| Eligibility Criteria | Inclusion Criteria: Main Inclusion Criteria:
Exclusion 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 | Not Provided | |||
| Removed Location Countries | Spain | |||
| Administrative Information | ||||
| NCT Number | NCT00895050 | |||
| Other Study ID Numbers | 0881X1-4576 B1801084 | |||
| Has Data Monitoring Committee | No | |||
| U.S. FDA-regulated Product | Not Provided | |||
| IPD Sharing Statement | Not Provided | |||
| Responsible Party | Director, Clinical Trial Disclosure Group, Pfizer, Inc | |||
| Study Sponsor | Pfizer | |||
| Collaborators | Not Provided | |||
| Investigators |
| |||
| PRS Account | Pfizer | |||
| Verification Date | July 2011 | |||