A Roentgen Stereophotogrammetric Analysis on Migration of Knee Prostheses.

Osteoarthritis Clinical Trial

— Ti-Tan  

Official title:

A Roentgen Stereophotogrammetric Analysis on Migration of Knee Prostheses. A Randomised Prospective Study of Tantalum Versus Titanium Implants.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00138853
• Other study ID #: 20030119
• Status: Completed
• Phase: N/A
• Start date: November 2003
• Est. completion date: April 2010

Study information

• Verified date: February 2020
• Source: University of Aarhus
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to compare the early migration of two uncemented total knee arthroplasties with different metal coating. Only the tibial prosthesis plateau varies. One is made out of tantalum and has two short pegs for fixation into the tibia while the other is covered by titanium fiber-mesh on the bone-near site and has 4 short pegs for screw fixation into the tibia.

Description:

Around 4% of total knee arthroplasties (TKA) are revised 15 years after the primary operation, most due to loosening of the implant. The use of uncemented prostheses are expected to extend the fixation time and thereby the years of TKA survival. When a cementless implant is inserted, direct bone ingrowth to the implant depends on a complete primary stabilisation. Movement between the bone and implant will cause a fibrous membrane leading to micromotions. Micromotions can be evaluated by radiophotogrammetric analysis (RSA) in early follow-up and they have been shown to be a prognostic marker for painful loosening of the implant.

Tantalum is a fairly new biomaterial designed with a high and bone-binding porosity. Tantalum has already proven to be a good prosthesis material facilitating fast bone-ingrowth and supplying mechanical qualities in the bone-prosthesis interface that surpasses the qualities of regular prosthesis materials by uncemented method. Titanium on the other hand has been used as a prosthesis coating for years and also promote prosthesis fixation by osteointegration.

The purpose of this study is to compare the early migration of two uncemented total knee implants with different metal coating and fixation method. Only the tibial prosthesis plateau varies in design. One plateau is a 2 pegged tantalum monobloc and the other plateau is a modular titanium fiber-mesh coating with 4 short pegs for screw fixation into the tibia.

Furthermore the extend of the expected micromovements between the polyethylene liner and the metal backing of the titanium plateau will be compared to the stable tantalum monobloc.

Theoretically tantalum should allow a more optimal coating for bone ingrowth, but as primary stability is also important for longterm prostheses survival the method of primary fixation could alså play a role.

To evaluate both the plateau-bone micromotions and the polyethylene-prosthesis micromovements metal markers have been placed on the prosthesis pre-operatively and furthermore into the tibial bone and into the tibial polyethylene during surgery allowing us to evaluate stereo x-rays by a photogrammetric analyses called RSA at the Orthopaedic Center, Aarhus University Hospital. Follow-up stereo x-rays will be scheduled for 1 week, 3 months, 6 month, 1 years, 2 years and 5 years post-surgery.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: April 2010
• Est. primary completion date: April 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Patients with one- or double-sided primary knee arthrosis.

2. Patients with a sufficient bone quality for implantation of an uncemented prosthesis.

3. Informed and written patient consent.

Exclusion Criteria:

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

2. Patients who peroperatively are estimated unsuitable for an uncemented knee arthroplasty e.g. due to bone cysts or dilution of the bone mass.

3. Patients who use non-steroid anti-inflammatory drugs (NSAID) and cannot refrain from taking them postoperatively (this includes COX-2-inhibitors).

4. Patients with osteoporosis estimated from the preoperative x-ray or former diagnosis of osteoporosis.

5. Patients with fracture sequelae.

6. Women, who are pregnant or are at risk of getting pregnant.

Related Conditions & MeSH terms

• Osteoarthritis

Intervention

Device:
• Tibial component
Tibial component inserted at the time of surgery

Locations

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

Sponsors (3)

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

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Polyethylene wear (mm) of the medial and lateral knee prosthesis compartments at 5 years followup measured with model-based radiostereometry		Up to 5 years
Secondary	Difference in MPTM (mm) tibial component migration from 2-5 years (stabilization 3) measured with model-based radiostereometry		up to 5 years
Secondary	Number of implants migrating above 0.2mm MTPM from 1-2 years (stabilization 2) and 2-5 years (stabilization 3) measured with model-based radiostereometry		Up to 5 years
Secondary	Osteolysis (radiolucent lines >1 mm) in the tibial periprosthetic region measured on radiographs		Up to 5 years