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Trial Comparing Navigated and Conventional Implantation Techniques in Knee Replacement Surgery

Primary Purpose

Osteoarthritis

Status
Unknown status
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
conventional vs. navigated total knee arthroplasty
Sponsored by
University Hospital Schleswig-Holstein
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis focused on measuring Osteoarthritis, Arthroplasty, Replacement, Knee, Instrumentation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients who are scheduled to receive a Total Knee Arthroplasty at the participating institutions for primary diagnosis of osteoarthritis are candidates for inclusion in the study.

Exclusion Criteria:

  • A history of septic arthritis in the joint to operate
  • Amputations
  • Neurological deficits
  • Inability to complete the questionnaires because of cognitive or language difficulties
  • Prior knee arthroplasty in the joint to operate
  • Prior arthroplasty in another weight-bearing joint within the last 6 months

Sites / Locations

  • University of Mannheim, Center for Orthopaedic Surgery and Traumatology
  • University of Regensburg, Department of Orthopaedic Surgery
  • University of Würzburg, Department of Orthopaedic SurgeryRecruiting
  • University of Cologne, Department of Orthopaedic Surgery
  • University of Schleswig-Holstein, Kiel Medical CenterRecruiting
  • Charité Universitätsmedizin Berlin, Center for Musculoskeletal SurgeryRecruiting
  • DIAKO Ev. Diakonie-Hospital gGmbH, Clinic for Orthopaedic Surgery and TraumatologyRecruiting
  • Schön-Klinikum Hamburg-Eilbek, Department of Orthopedic Surgery and Traumatology

Outcomes

Primary Outcome Measures

Physical functioning as measured with the Western Ontario and McMasters osteoarthritis index

Secondary Outcome Measures

Leg-specific pain and stiffness as measured with the WOMAC
The Lequesne Knee Score
The physical component summary of the SF-36
EuroQoL-5D
Patient satisfaction
Balance abilities as investigated with the Biodex Stability System®
Motoric coordination as assessed by a shortened version of the "Dortmunder modified Romberg Test for Seniors"
Proprioception assessed according to guidelines established by Barrack and Swanik
Axis relations evaluated by postoperative standardized lateral and AP X-rays

Full Information

First Posted
February 2, 2007
Last Updated
April 23, 2007
Sponsor
University Hospital Schleswig-Holstein
Collaborators
DePuy International
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1. Study Identification

Unique Protocol Identification Number
NCT00431509
Brief Title
Trial Comparing Navigated and Conventional Implantation Techniques in Knee Replacement Surgery
Official Title
A Randomized Trial Comparing Navigated and Conventional Implantation Techniques in Knee Replacement Surgery. Influence on Operative Result, Health-Related Quality of Life, and Coordinative Abilities.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2007
Overall Recruitment Status
Unknown status
Study Start Date
January 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2009 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital Schleswig-Holstein
Collaborators
DePuy International

4. Oversight

5. Study Description

Brief Summary
This study is undertaken to investigate the effect of navigated knee implantation surgery on physical function, joint stiffness, pain, quality of life and coordinative abilities. One group of patients will receive navigated knee implantation surgery, the other traditional knee implantation surgery, without use of the navigation system. The study is designed as a randomized trial. That means that all patients who have given their consent to participate in this study will be allocated to either navigated or conventional surgery by chance. A total of 477 patients will be included in this study and will be followed up for 12 month. In this period all patients will be asked to fill in functional and quality of life questionnaires at baseline, 6 weeks and 3, 6 and 12 month follow-up. Coordinative abilities will be evaluated once in the time-frame 3 to 6 months postoperatively.
Detailed Description
Various risk factors influencing the success of Total Knee Arthroplasty (TKA) have been studied. Today age, gender, primary or revision surgery, comorbidities and baseline characteristics are known to influence the health-related quality of life after TKA. It is thought, that accurate mechanical alignment and ligament balance ensure optimal kinematic performance and wear, which in turn improves long-term outcome. During preparation of the bone for the implantation of the knee prosthesis, numerous cuts are performed. Traditionally mechanical adjusted jigs are used to accurately align and position the instruments. Since this alignment process is a source for deviation even in experienced surgeons, several navigation systems were developed. Using these systems, the surgeon is guided in the location of the instruments with the help of a computer. Several studies could show that the use of such a navigation system leads to an improved execution of planned axis relations, as measured on the radiographs. However, it is not clear, whether or to what extent the improved realization of the preoperative planned axis relations results in a positive effect for the patient. This multicenter randomized clinical trail is conducted to compare the operative results of navigated and non-navigated knee replacement surgery. The aim of this study is to evaluate the use of a navigation system on health-related quality of life, measured as pain, stiffness, physical function, coordinative abilities, and patient satisfaction. The hypotheses tested is that the use of the navigation system for total knee arthroplasty leads to improved health-related quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis
Keywords
Osteoarthritis, Arthroplasty, Replacement, Knee, Instrumentation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
477 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
conventional vs. navigated total knee arthroplasty
Primary Outcome Measure Information:
Title
Physical functioning as measured with the Western Ontario and McMasters osteoarthritis index
Secondary Outcome Measure Information:
Title
Leg-specific pain and stiffness as measured with the WOMAC
Title
The Lequesne Knee Score
Title
The physical component summary of the SF-36
Title
EuroQoL-5D
Title
Patient satisfaction
Title
Balance abilities as investigated with the Biodex Stability System®
Title
Motoric coordination as assessed by a shortened version of the "Dortmunder modified Romberg Test for Seniors"
Title
Proprioception assessed according to guidelines established by Barrack and Swanik
Title
Axis relations evaluated by postoperative standardized lateral and AP X-rays

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients who are scheduled to receive a Total Knee Arthroplasty at the participating institutions for primary diagnosis of osteoarthritis are candidates for inclusion in the study. Exclusion Criteria: A history of septic arthritis in the joint to operate Amputations Neurological deficits Inability to complete the questionnaires because of cognitive or language difficulties Prior knee arthroplasty in the joint to operate Prior arthroplasty in another weight-bearing joint within the last 6 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thoralf R Liebs, Dr.
Phone
+49 431 597
Ext
2444
Email
liebs@orthop.uni-kiel.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joachim Hassenpflug, Prof. Dr.
Organizational Affiliation
University of Schleswig-Holstein, Kiel Medical Center
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Thoralf R Liebs, Dr.
Organizational Affiliation
University of Schleswig-Holstein, Kiel Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Mannheim, Center for Orthopaedic Surgery and Traumatology
City
Mannheim
State/Province
Baden-Wuerttemberg
ZIP/Postal Code
68167
Country
Germany
Individual Site Status
Not yet recruiting
Facility Name
University of Regensburg, Department of Orthopaedic Surgery
City
Bad Abbach
State/Province
Bavaria
ZIP/Postal Code
93077
Country
Germany
Individual Site Status
Suspended
Facility Name
University of Würzburg, Department of Orthopaedic Surgery
City
Würzburg
State/Province
Bavaria
ZIP/Postal Code
97074
Country
Germany
Individual Site Status
Recruiting
Facility Name
University of Cologne, Department of Orthopaedic Surgery
City
Cologne
State/Province
Northrhine-Westfalia
ZIP/Postal Code
50924
Country
Germany
Individual Site Status
Not yet recruiting
Facility Name
University of Schleswig-Holstein, Kiel Medical Center
City
Kiel
State/Province
Schleswig-Holstein
ZIP/Postal Code
24105
Country
Germany
Individual Site Status
Recruiting
Facility Name
Charité Universitätsmedizin Berlin, Center for Musculoskeletal Surgery
City
Berlin
ZIP/Postal Code
10117
Country
Germany
Individual Site Status
Recruiting
Facility Name
DIAKO Ev. Diakonie-Hospital gGmbH, Clinic for Orthopaedic Surgery and Traumatology
City
Bremen
ZIP/Postal Code
28239
Country
Germany
Individual Site Status
Recruiting
Facility Name
Schön-Klinikum Hamburg-Eilbek, Department of Orthopedic Surgery and Traumatology
City
Hamburg
ZIP/Postal Code
22081
Country
Germany
Individual Site Status
Not yet recruiting

12. IPD Sharing Statement

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Trial Comparing Navigated and Conventional Implantation Techniques in Knee Replacement Surgery

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