AzTrials
AzTrials

Arthroplasty; Replacement; KneeNCT04037228

Surgical Outcomes of the Accelerometer-based Navigation System for Total Knee Arthroplasty

An observational study of Arthroplasty; Replacement; Knee and Radiotherapy; Image-Guided, run by Chinese University of Hong Kong at 1 site in Hong Kong.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

Osteoarthritis (OA) is a very common condition in the elderly population. Treatment for end-stage OA is total knee Replacement (TKR) Read more about this study

Who is it for?
Any age
What is being tested?
KneeAlign 2 system (OrthAlign Inc, Aliso Viejo, California)
Type of treatment
Medical device
How many people
40 participants
Where
1 siteHong Kong
Study dates
30 Apr 2020to 31 Dec 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Osteoarthritis knee patients in hospital

Who may be able to join

  • Male and female subjects aged over 18 years old
  • All patients must provide their written consent
  • patients with a history of osteoarthritis, rheumatoid arthritis, or post-traumatic arthritis who will receive a primary, posterior-stabilized TKA.
  • All patients should have at least 8 years of school education;
  • Radiological evidence of osteoarthritis with Kellgren and Lawrence grade 2 or above

Who cannot join

  • Patients are planned to receive a unicondylar or patellofemoral arthroplasty.
  • Patients with previous cases of alcoholism or drug abuse;
  • Pregnancy and breast-feeding;
  • Presence of serious pathologies;
  • revision surgery
  • Knee infection
  • Non-consenting patients who have not provided the written Informed Consent;
  • Mechanical instability, ligamentous laxity/deficiency and gross deformity

Trial locations and contacts

1 site in 1 country.

Hong Kong1 site, 1 recruiting
  • Department of Orthopaedics & Traumatology

    Hong Kong

    Ki Wai Ho, MBChB, MSc, MRCSEd, FRCSEd, (852)35052715, kevinho@cuhk.edu.hk

    Ki Wai Ho, MBChB, MSc, MRCSEd, FRCSEd

    Recruiting

Other trials in Hong Kong

About this study

Osteoarthritis (OA) is a very common condition in the elderly population. Treatment for end-stage OA is total knee Replacement (TKR)

Read the detailed description

Overall the success rate of TKR is very high with high patient satisfaction and outcomes. Survivorship depends on patient selection and surgical techniques. Femoral and tibial component mal-alignment might lead to early failure.

Although recent studies have questioned the significance of overall postoperative mechanical alignment on survivorship, most studies still demonstrate alignment to be a crucial factor in the clinical success of TKA [1]. Ritter et al [2], in a review of 6070 TKAs, noted the risk of aseptic failure to significantly increase with a tibial component orientation less than 90° relatives to the tibial axis and a femoral component orientation greater than 8° of valgus relative to the femoral axis (failure rate, 8.7%).

Berend et al [3], in a review of 3152 TKAs, demonstrated that a tibial varus alignment of greater than 3° increased the odds of implant failure and medial bone collapse by roughly 17 times.

The most commonly used methods of component alignment in TKA are an extramedullary (EM) alignment guide for the tibial resection and an intramedullary (IM) alignment guide for the distal femoral resection. Unfortunately, these "conventional" methods have demonstrated a limited degree of accuracy for both overall mechanical alignment and individual component Method to create an even more accurate resection includes the use computer-assisted navigation technique. In a meta-analysis of 29 studies comparing computer assisted surgical (CAS) to conventional techniques in TKA (Mason et al). The authors found that only 68.2% of TKAs in the conventional group achieved an overall mechanical axis within 3° of neutral (vs 91.0% in the CAS group), 65.9% achieved a femoral varus/valgus alignment within 2° of perpendicular to the femoral mechanical axis (vs 90.4% in the CAS group) and 79.7% achieved a tibial varus/valgus alignment within 2° of perpendicular to the tibial mechanical axis (vs 95.2% in the CAS group).

However, despite these advantages, concerns regarding increased capital costs, operative times, extra pin sites, and the learning curve associated with the use of CAS techniques have continued to limit its widespread acceptance.

Another factor that might have limited its usage is that so far no study has shown the accuracy with CAS can directly lead to a longer survivorship of the implant or a better functional outcome. However, the most surgeon still believes a correct align knee will yield a better function and outcome.

This shed the light to a new navigation device. Iorio et.al [4]The KneeAlign 2 system (OrthAlign Inc, Aliso Viejo, California) is an accelerometer-based, portable navigation device for TKA that attempts to combine the alignment accuracy of large-console CAS systems, with the ease of use and convenience of conventional alignment methods. It is used to perform the proximal tibial and distal femoral resections in TKA. It does not require the use of a large console for registration and alignment feedback and is compatible with any TKA system. It consists of a disposable display console (2 × 4 × 2 inches in size) and a reference sensor, both of which are used for the tibial and femoral resections The KneeAlign 2 is the second version of the KneeAlign originally developed to perform only the proximal tibia resection in TKA. The KneeAlign 2 required the additional design of a femoral jig and cutting block and allows for the use of the same display console to perform both the proximal tibia and distal femur resections. The display console and reference sensor each contains triaxial accelerometers that communicate wirelessly with one another. The surgical technique for using the KneeAlign 2 to perform the tibial resection is the same as previously described Briefly, the tibial jig has 2 primary components (a fixed component and a mobile component) connected by a proximal articulation .The fixed component, with the attached reference sensor, is first pinned to the tibia. The purpose of the fixed component is to account for the movement of the tibia during cutting block alignment.

Being tested
KneeAlign 2 system (OrthAlign Inc, Aliso Viejo, California)

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • KneeAlign 2 system (OrthAlign Inc, Aliso Viejo, California)Device

    The KneeAlign 2 system (OrthAlign Inc, Aliso Viejo, California) is an accelerometer-based, portable navigation device for TKA that attempts to combine the alignment accuracy of large-console CAS systems, with the ease of use and convenience of conventional alignment methods. It is used to perform the proximal tibial and distal femoral resections in TKA. It consists of a disposable display console (2 × 4 × 2 inches in size) and a reference sensor, both of which are used for the tibial and femoral resections The display console and reference sensor each contains triaxial accelerometers that communicate wirelessly with one another. Briefly, the tibial jig has 2 primary components (a fixed component and a mobile component) connected by a proximal articulation .The fixed component, with the attached reference sensor, is first pinned to the tibia. The purpose of the fixed component is to account for the movement of the tibia during cutting block alignment.

Study groups in NCT04037228
Study groupRoleWhat they receive
KneeAlign 2Those of the group will be adopt KneeAlign 2: accelerometer-based navigation system at total knee arthroplasty.
Receives: Device: KneeAlign 2 system (OrthAlign Inc, Aliso Viejo, California)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes of Radiological Assessments of the knees at baseline

    Standing antero-posterior (AP) hip-knee-ankle (HKA) and lateral knee-to-ankle radiographs will be performed to determine the varus/valgus alignment and the posterior slope of the tibial components relative to the mechanical axis.

    Measured: Through study completion, an average of 1 year

  2. Changes of Radiological Assessments of the knees post-operatively

    Standing antero-posterior (AP) hip-knee-ankle (HKA) and lateral knee-to-ankle radiographs will be performed to determine the varus/valgus alignment and the posterior slope of the tibial components relative to the mechanical axis.

    Measured: Through study completion, an average of 1 year

Secondary outcomes (1)
  1. Knee Functions measure by the Knee Society Score

    Questionnaire - Physician will assess on the Visual Analog Scale in pain score (None to Severe), Flexion Contracture (None to >20°), Extension lag (None to 20°), Total Range of Flexion (0-5° to 121-125°), Alignment (0° to Over 15°), Antero-posterior stability (<5mm to 10+mm), Mediolateral stability (<5° to 15°). Patients will record individuals' satisfaction, functional activities, and expectations.

    Measured: Through study completion, an average of 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Jul 2019
  2. Study start30 Apr 2020
  3. Primary completion31 Dec 2024 (estimated)
  4. Study completion31 Dec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04037228
Sponsor's protocol ID
2017.458
Status last verified
Dec 2023
First submitted
20 Jun 2019
Last updated
7 Dec 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Arthroplasty; Replacement; Knee and Radiotherapy; Image-Guided, run by Chinese University of Hong Kong at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 7 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes of Radiological Assessments of the knees at baseline (time frame: Through study completion, an average of 1 year). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Dec 2023.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in