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| Tracking Information | |||||||||
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| First Received Date † | September 9, 2005 | ||||||||
| Last Updated Date | October 15, 2008 | ||||||||
| Start Date † | January 2001 | ||||||||
| Current Primary Outcome Measures † | |||||||||
| Original Primary Outcome Measures † | |||||||||
| Change History | Complete list of historical versions of study NCT00163228 on ClinicalTrials.gov Archive Site | ||||||||
| Current Secondary Outcome Measures † | |||||||||
| Original Secondary Outcome Measures † | |||||||||
| Descriptive Information | |||||||||
| Brief Title † | Functional Evaluation of the Total Knee Prostheses:Rising From a Chair | ||||||||
| Official Title † | Functional Evaluation of Total Knee Arthroplasties,Protocol for Rising From a Chair. | ||||||||
| Brief Summary | In this study, a functional evaluation of total knee arthroplasty (TKA) patients is performed. The patients are measured prior to surgery and 6 and 12 months after surgery. The measurements consist of questionnaires and rising from a chair. Also, two types of TKA are functionally evaluated. At last, the TKA group will be compared to a THP group. |
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| Detailed Description | |||||||||
| Study Phase | |||||||||
| Study Type † | Observational | ||||||||
| Study Design † | Other, Prospective | ||||||||
| Condition † |
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| Intervention † | |||||||||
| Study Arms / Comparison Groups | |||||||||
| Publications * | |||||||||
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status † | Withdrawn | ||||||||
| Enrollment † | 100 | ||||||||
| Estimated Completion Date | May 2007 | ||||||||
| Primary Completion Date | |||||||||
| Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||
| Ages | |||||||||
| Accepts Healthy Volunteers | Yes | ||||||||
| Contacts †† | |||||||||
| Location Countries † | Netherlands | ||||||||
| Expanded Access Status | |||||||||
| Administrative Information | |||||||||
| NCT ID † | NCT00163228 | ||||||||
| Responsible Party | |||||||||
| Secondary IDs †† | FBW Stratec 96856 | ||||||||
| Study Sponsor † | Radboud University | ||||||||
| Collaborators †† | Johnson & Johnson, Leeds, UK | ||||||||
| Investigators † |
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| Information Provided By | Radboud University | ||||||||
| Verification Date | October 2008 | ||||||||
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† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |
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