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Correlation Between Alignment of Lower Limb and Clinical Outcome After Total Knee Prosthesis.

This study is not yet open for participant recruitment. (see Contacts and Locations)
Verified August 2012 by University Hospital, Ghent
Sponsor:
Information provided by (Responsible Party):
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT01666873
First received: August 14, 2012
Last updated: August 16, 2012
Last verified: August 2012

August 14, 2012
August 16, 2012
September 2012
January 2016   (final data collection date for primary outcome measure)
  • Clinical results after total knee prosthesis with standardized questionnaires after 6 months [ Time Frame: 6 months after total knee prosthesis ] [ Designated as safety issue: No ]
    Standardized questionnaires (KOOS KSS en Oxford knee score-questionnaire).
  • Clinical results after total knee prosthesis with standardized questionnaires after 12 months. [ Time Frame: 12 months after total knee prosthesis ] [ Designated as safety issue: No ]
    Standardized questionnaires (KOOS KSS en Oxford knee score-questionnaire).
  • Clinical results after total knee prosthesis with standardized questionnaires after 24 months. [ Time Frame: 24 months after total knee prosthesis ] [ Designated as safety issue: No ]
    Standardized questionnaires (KOOS KSS en Oxford knee score-questionnaire).
Same as current
Complete list of historical versions of study NCT01666873 on ClinicalTrials.gov Archive Site
Alignment of lower limb, slope of lateral and medial tibial plateau, femoral slope. [ Time Frame: 6 months after total knee prosthesis ] [ Designated as safety issue: No ]
imaging with 3D software (MIMICS)
Same as current
Not Provided
Not Provided
 
Correlation Between Alignment of Lower Limb and Clinical Outcome After Total Knee Prosthesis.
Correlation Between Alignment of Lower Limb and Clinical Outcome After Total Knee Prosthesis.

Evaluation of the clinical results after total knee prosthesis, and correlation with the alignment of the lower limb.

Radiological measurements by means of 3D technology will be performed. The clinical result will be stipulated by means of standardized questionnaires (KOOS, KSS and Oxford knee score-questionnaire).

Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

People who have osteoarthritis of the knee joint and receive a total knee prosthesis.

Osteoarthritis of the Knee Joint
Procedure: patients that undergo a total knee prosthesis
total knee prosthesis
Patients that undergo a total knee prosthesis.
Intervention: Procedure: patients that undergo a total knee prosthesis
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
150
May 2016
January 2016   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patient with osteoarthritis of the knee joint, without severe bone deformation

Exclusion Criteria:

  • none
Both
Not Provided
No
Contact: Jan Victor, MD, PhD Jan.Victor@ugent.be
Belgium
 
NCT01666873
2012/526
No
University Hospital, Ghent
University Hospital, Ghent
Not Provided
Principal Investigator: Jan Victor, MD, PhD Ghent University Hospital
University Hospital, Ghent
August 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP