![]() |
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
Tracking Information | |||||||||
---|---|---|---|---|---|---|---|---|---|
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. |
||||||||
Detailed Description | |||||||||
Study Phase | |||||||||
Study Type † | Observational | ||||||||
Study Design † | Other, Prospective | ||||||||
Condition † |
|
||||||||
Intervention † | |||||||||
Study Arms / Comparison Groups | |||||||||
Publications * | |||||||||
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
|||||||||
Recruitment Information | |||||||||
Recruitment Status † | Withdrawn | ||||||||
Enrollment † | 100 | ||||||||
Estimated Completion Date | May 2007 | ||||||||
Primary Completion Date | |||||||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
|
||||||||
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 † |
|
||||||||
Information Provided By | Radboud University | ||||||||
Verification Date | October 2008 | ||||||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |