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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00163228
Other study ID # FWB Stratec 96856
Secondary ID FBW Stratec 9685
Status Withdrawn
Phase N/A
First received September 9, 2005
Last updated October 15, 2008
Start date January 2001
Est. completion date May 2007

Study information

Verified date October 2008
Source Radboud University
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 100
Est. completion date May 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- unilateral TKA

Exclusion Criteria:

- TKA bilateral

- recent THP

- movement disorders like Parkinson's disease, insults, that disturb equilibrium and movements

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Netherlands ORL, Radboud University Nijmegen Medical Centre Nijmegen

Sponsors (2)

Lead Sponsor Collaborator
Radboud University Johnson & Johnson, Leeds, UK

Country where clinical trial is conducted

Netherlands, 

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