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Osteoarthritis, KneeNCT02444663

Validation of a Stress Device for the Knee

A study testing Clinician Valgus, Clinician Varus and Device Valgus - 0 Newton in people with Osteoarthritis, Knee, run by Oxford University Hospitals NHS Trust.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

X-rays are the most frequently used imaging test when evaluating the knee for joint replacement. They are non-invasive, safe and cost effective. They allow assessment of: progression of disease, appropriateness for joint replacement (in particular unicompartmental knee replacement (UKR)) as well as likely prognosis… Read more about this study

Who is it for?
Ages 50 years and older
Conditions the study is for
Osteoarthritis, Knee
What is being tested?
Clinician Valgus, Clinician Varus and Device Valgus - 0 Newton
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
9 participants
Where
No sites listed yet
Study dates
13 Jan 2016to 14 Dec 2016
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

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 50 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Participant is willing and able to give informed consent for participation in the study.
  • Male or Female, aged 50 years or above.
  • Knee osteoarthritis any grade, affecting the tibio-femoral joint
  • In the Investigator's opinion, is able and willing to comply with all trial requirements.
  • Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the trial.

Who cannot join

  • Previous joint replacement on ipsilateral knee
  • Previous anterior cruciate ligament reconstruction or injury
  • Previous high tibial osteotomy
  • Previous intra-articular fracture
  • History of Inflammatory arthritis

About this study

Official title: Validation of a Device for Performing Valgus and Varus Stress X-rays of the Knee

X-rays are the most frequently used imaging test when evaluating the knee for joint replacement. They are non-invasive, safe and cost effective. They allow assessment of: progression of disease, appropriateness for joint replacement (in particular unicompartmental knee replacement (UKR)) as well as likely prognosis following replacement.

Currently standard assessment involves: standing anteroposterior, lateral and skyline X-ray views. In addition in patients being considered for joint replacement valgus/varus stress X-rays are used to evaluate the lateral compartment (as well as medial collateral ligament) and medial compartment respectively to assess the status of the cartilage. Stress X-rays require the clinician to attend X-ray, often during busy clinics, exposing them to additional radiation, and as such they are seldom performed.

Read more

A patient and user friendly device for performing valgus and varus stress X-rays of the knee for diagnostic and pre-operative planning purposes in the setting of knee replacement surgery has been developed. This device has the potential to benefit patients as it will allow an accurate assessment of the pattern and severity of arthritis affecting their knee without the need for additional diagnostics such as MRI or arthroscopy. Furthermore for healthcare practitioners and providers this device will facilitate the smooth running of clinics and reduce the additional clinic appointments required to review MRI results. Ultimately this device will allow an informed discussion about treatment options, reduce the pre-operative uncertainty about suitability for UKR in those undergoing surgery and ensure that those patients who are suitable for UKR benefit from this procedure. This device will help ensure that patients receive the optimum treatment in a clinically and cost efficient manner.

This study will validate valgus and varus stress X-rays performed using the investigators' device against the gold standard of clinician performed manual stress.

Read the detailed description

X-rays are the most frequently used imaging test when evaluating the knee for joint replacement. They are non-invasive, safe and cost effective. They allow assessment of: progression of disease, appropriateness for joint replacement (in particular unicompartmental knee replacement (UKR)) as well as likely prognosis following replacement.

Currently standard assessment involves: standing anteroposterior, lateral and skyline X-ray views. In addition in patients being considered for joint replacement valgus/varus stress X-rays are used to evaluate the lateral compartment (as well as medial collateral ligament) and medial compartment respectively to assess the status of the cartilage.

The assessment of pattern and severity of disease is critical when evaluating suitability for joint replacement and well as when deciding between total knee replacement (TKR), where all articulating surface are replaced, or UKR, where only the diseased portion of the joint is replaced. Understanding the pattern of disease is essential to ensure appropriate patient selection for UKR, which is appropriate in up to half of patients undergoing knee replacement, and has significant benefits over TKR including: half the risk of venous thromboembolism, myocardial infarction or deep infection, two thirds the risk of stroke, one quarter the risk of blood transfusion and significantly lower mortality up to eight years following their operation.

Stress X-rays are currently performed by the clinician, requiring them to attend radiology, often during clinic. To perform the stress views the clinician fixes the knee and moves the tibia away from the midline, valgus stress, where an X-ray is taken. The alignment of this view is confirmed before the tibia is moved towards the midline, varus stress, where another X-ray is taken. Stress X-rays are resource dependent and can be time consuming. In addition, the technique can be uncomfortable for patients as well as resulting in additional radiation exposure to the clinical practitioner. On an average, a knee surgeon may be exposing themselves to excess of 300 exposures every year with the cumulative effect of radiation exposure being significant. As such in many centers stress views are often not performed, and as standing antero-posterior X-ray views are inadequate to assess disease severity and pattern many clinicians have adopted additional imaging modalities such as MRI or direct observation via arthroscopy to evaluate the status of the cartilage in each compartment. The use of these additional imaging techniques introduces significant additional costs as well as delays to treatment. Furthermore the long term outcomes of UKR have been established using stress views, and as a consequence outcomes based on MRI or arthroscopic findings have not been fully established.

A patient and user friendly device for performing valgus and varus stress X-rays of the knee for diagnostic and pre-operative planning purposes in the setting of knee replacement surgery has been developed. This device has the potential to benefit patients as it will allow an accurate assessment of the pattern and severity of arthritis affecting their knee without the need for additional diagnostics such as MRI or arthroscopy. Furthermore for healthcare practitioners and providers this device will facilitate the smooth running of clinics and reduce the additional clinic appointments required to review MRI results. Ultimately this device will allow an informed discussion about treatment options, reduce the pre-operative uncertainty about suitability for UKR in those undergoing surgery and ensure that those patients who are suitable for UKR benefit from this procedure. This device will help ensure that patients receive the optimum treatment in a clinically and cost efficient manner.

This study will validate valgus and varus stress X-rays performed using the investigators' device against the gold standard of clinician performed manual stress.

Being tested
Clinician Valgus, Clinician Varus, Device Valgus - 0 Newton, Device Valgus - 10 Newton, Device Valgus - 20 Newton
Medical subject headings
Osteoarthritis, Knee

What participants receive

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

  • Clinician ValgusRadiation

    Clinician performed valgus stress X-ray under fluoroscopy

  • Clinician VarusRadiation

    Clinician performed varus stress X-ray under fluoroscopy

  • Device Valgus - 0 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed valgus stress X-ray under fluoroscopy.

  • Device Valgus - 10 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed varus stress X-ray under fluoroscopy.

  • Device Valgus - 20 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed valgus stress X-ray under fluoroscopy.

  • Device Valgus - 30 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed valgus stress X-ray under fluoroscopy.

  • Device Varus - 0 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed valgus stress X-ray under fluoroscopy.

  • Device Varus - 10 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed valgus stress X-ray under fluoroscopy.

  • Device Varus - 20 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed valgus stress X-ray under fluoroscopy.

  • Device Varus - 30 NewtonRadiation

    Device (Oxford Stress System for Knee Arthroplasty Radiographs (OSSKAR)) performed valgus stress X-ray under fluoroscopy.

Study groups in NCT02444663
Study groupRoleWhat they receive
Clinician ValgusActive comparatorClinician performed fluoroscopic valgus and varus stress X-rays
Receives: Radiation: Clinician Valgus
Clinician VarusActive comparatorClinician performed fluoroscopic varus stress X-rays
Receives: Radiation: Clinician Varus
Device Valgus - 0 Newton forceExperimentalDevice performed fluoroscopic valgus stress X-rays - 0 Newton force
Receives: Radiation: Device Valgus - 0 Newton
Device Valgus - 10 Newton forceExperimentalDevice performed fluoroscopic valgus stress X-rays - 10 Newton force
Receives: Radiation: Device Valgus - 10 Newton
Device Valgus - 20 Newton forceExperimentalDevice performed fluoroscopic valgus stress X-rays - 20 Newton force
Receives: Radiation: Device Valgus - 20 Newton
Device Valgus - 30 Newton forceExperimentalDevice performed fluoroscopic valgus stress X-rays - 30 Newton force
Receives: Radiation: Device Valgus - 30 Newton
Device Varus - 0 Newton forceExperimentalDevice performed fluoroscopic varus stress X-rays - 0 Newton force
Receives: Radiation: Device Varus - 0 Newton
Device Varus - 10 Newton forceExperimentalDevice performed fluoroscopic varus stress X-rays - 10 Newton force
Receives: Radiation: Device Varus - 10 Newton
Device Varus - 20 Newton forceExperimentalDevice performed fluoroscopic varus stress X-rays - 20 Newton force
Receives: Radiation: Device Varus - 20 Newton
Device Varus - 30 Newton forceExperimentalDevice performed fluoroscopic varus stress X-rays - 30 Newton force
Receives: Radiation: Device Varus - 30 Newton

What is being measured

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

  1. Compartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)

    Knee minimum joint space width measured on anteroposterior fluoroscopic images using custom, validated, in house software (KneeMorph, MATLAB, MathWorks, Massachusetts).

    Measured: Day 0

Secondary outcomes (1)
  1. Pain (VAS 0 - 10)

    Pain Score during stress radiographs (VAS 0 - 10) where a higher score represents more pain (10 = worst pain).

    Measured: At time of procedure

Timeline

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

  1. First posted14 May 2015 (estimated)
  2. Study start13 Jan 2016
  3. Primary completion14 Dec 2016
  4. Study completion14 Dec 2016

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Non-randomised
Intervention model
Crossover
Model description
Participants will have the interventions in each of the ten arms of the study.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
9 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02444663
Sponsor's protocol ID
109367
Status last verified
Oct 2021
First submitted
27 Apr 2015
Last updated
4 Nov 2021
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Clinician Valgus, Clinician Varus and Device Valgus - 0 Newton in people with Osteoarthritis, Knee, run by Oxford University Hospitals NHS Trust.

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 5 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: finished, as of the sponsor's last update on 4 Nov 2021. Status can change between updates, so confirm with the study contact before making plans.

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?

Yes. Results are posted in the registry (first posted 4 Nov 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Compartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment) (time frame: Day 0). 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 4 Nov 2021.

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Validation of a Stress Device for the Knee | AzTrials