Oxford Partial Knee Replacement. A Randomized Clinical Trial of Three Implant Types

Osteoarthritis, Knee Clinical Trial

Official title:

Oxford Partial Knee Replacement: A Randomized Clinical Trial of Three Implant Types.

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00679120
• Other study ID #: 20070258
• Status: Active, not recruiting
• Phase: N/A
• Start date: May 2009
• Est. completion date: August 2024

Study information

• Verified date: December 2022
• Source: University of Aarhus
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this scientific study is to clarify whether there is a relationship between the appearance of radiolucent lines in bone-cement interphase of the tibial component of the different models of the Oxford Uni Knee prosthesis and poor prognosis of these prostheses. This will be accomplished in a se-ries of three different Oxford Uni Knees.

Description:

The purpose of this scientific study is to clarify whether there is a relationship between the appearance of radiolucent lines in bone-cement interphase of the tibial component of the different models of the Oxford Uni Knee prosthesis and poor prognosis of these prostheses. This will be accomplished in a series of three different Oxford Uni Knees by studying:

1. Three way randomized comparison of migration (prosthetic fixation) by Model Based RSA with three different Oxford Uni Knee prosthesis (both tibial trays and femoral components will be assessed).

2. Fluoroscopy (screening) roentgenograms for determination of RLL around the tibial component and "overhang" of the tibial trays.

3. Changes in periprosthetic bone mineral density between the three randomized groups evaluated in the proximal tibia and distal femur on the surgical side and on the unaffected tibial condyle area (BMD).

4. Clinical function of the Uni Knee evaluated by a score system using a recent Danish adaptation of the Oxford Knee Score that consists of a questionnaire filled-out by the patient with 12 simple questions on pre-and postoperative assessment of the ADL.

5. Analysis of wear of the mobile polyethylene (meniscus) including a methodical study as to whether the technique requires weightbearing (standing) stereoroentgenograms or whether non-weightbearing stereoroentgenograms can be used (assessed with Model Based RSA).

6. If a fast bone-remodeling increases the risk of aseptic loosening (histomorphometric results combined with RSA results and possible revision)

7. Increased risk of aseptic loosening with cemented (two designs) compared to uncemented im-plants.

8. If bone-remodeling of the proximal tibia is dependent on gender and age.

The study would be considered a success if all designs of the prostheses are firmly fixed and remain so during the entire period of study, that is, no increasing migration is seen using RSA. It would be a success if the appearance of RLL beneath the implant in the proximal tibia is unrelated to bone loss and prosthesis migration.

The hypotheses are:

1. RLL in relation to the tibial component is unimportant for fixation of the Oxford Uni Knee as assessed with DEXA and RSA.

2. There is very little wear of the polyethylene in the course of a 5 year follow-up as assessed with RSA.

3. The femoral component is expected to remain fixed throughout the entire period of follow-up.

4. Function assessment as ROM (range of motion) after UKA is satisfactory and generally better than after TKA.

5. All three prosthetic designs are expected to migrate minimally and remain fixed throughout the follow-up period, but the uncemented design is expected to be superior to the cemented design.

6. No difference in clinical outcome between the three prosthetic types.

7. The bone-remodeling rate in the medial periarticular tibia bone increases the risk of aseptic loosening.

The primary parameters of effect are RLL, RSA and DEXA. The secondary parameters of effect are bone-remodeling, wear analysis, Oxford Knee Score (ADL) and ROM.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 75
• Est. completion date: August 2024
• Est. primary completion date: October 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients, both men and women, with anteromedial unicompartmental knee osteoarthritis

2. Patients found suitable for UKA with telos stress-radiographs

3. Patients with sufficient bone quality to allow insertion of a Uni Knee prosthesis

4. Patellofemoral osteoarthritis is not a contraindication if the patient does not have symptoms from the patellofemoral joint

5. Patients can only take part in one knee study

6. All age groups, in good condition and responsible adults

7. Informed, written compliance consent.

Exclusion Criteria:

1. Patients with neuromuscular or vascular diseases in the affected leg

2. Patients found to be unsuitable for UKA before or at surgery

3. Preoperative extensions defect greater than 10 degrees

4. Preoperative maximal flection of less than 100 degrees

5. Symptomatic patellofemoral osteoarthritis

6. Insufficiency with regard to ACL

7. Patients templated to a size XS or XL femoral component prior to surgery.

8. Patients with osteoporosis on the basis of preoperative x-rays or earlier diagnosis

9. Continuous medical treatment with vitamin K antagonist (Warfarin), known to reduce bone mass in general by a factor of 5

10. Patients with fracture sequelae (intraarticular fracture and all tibial condyle fractures)

11. Patients previous having PTO or other extensive knee surgery

12. Patients with metabolic bone disease

13. Patients with rheumatoid arthritis

14. Postmenopausal female patients being treated with systemic hormonal substitution (not taking into local vaginal treatment)

15. Patients who intermittently or continuously require treatment with systemic glucocorticoids

16. Non-Danish citizens

17. Insufficient command of the Danish language (read and speak)

18. Senile dementia

19. Misuse of drugs or Alcohol

20. Serious psychiatric illness

21. Disseminated malignant disease (cancer) and treatment with radiation or chemotherapy

22. Serious systemic disease (e.g.. hemiparesis and severe Parkinsonism)

23. Systemic hip or back condition

24. Employed by the department of orthopaedic surgery

25. On-going case involving work injury of the knee

26. Patients with poor dental status

Related Conditions & MeSH terms

• Osteoarthritis, Knee

Intervention

Device:
• Oxford Uni Knee
Oxford Uni Knee inserted at the time of surgery
• Oxford Uni Knee
Oxford Uni Knee inserted at the time of surgery
• Oxford Uni Knee
Oxford Uni Knee inserted at the time of surgery (porous coated and HA coated)

Locations

Country	Name	City	State
Denmark	Orthopaedic Center, Aarhus University Hospital	Aarhus

Sponsors (4)

Lead Sponsor	Collaborator
University of Aarhus	Aarhus University Hospital, Vejle Hospital, Zimmer Biomet

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Three way randomized comparison of migration (prosthetic fixation) by Model Based RSA with three different Oxford Uni Knee prosthesis (both tibial trays and femoral components will be assessed)		2016
Secondary	Fluoroscopy (screening) roentgenograms for determination of RLL around the tibial component and "overhang" of the tibial trays.		2016