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Validation of a Stress Device for the Knee

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02444663
Enrollment
9
Registered
2015-05-14
Start date
2016-01-13
Completion date
2016-12-14
Last updated
2021-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Knee

Brief 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 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. 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.

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.

Interventions

RADIATIONClinician Valgus

Clinician performed valgus stress X-ray under fluoroscopy

RADIATIONClinician Varus

Clinician performed varus stress X-ray under fluoroscopy

RADIATIONDevice Valgus - 0 Newton

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

RADIATIONDevice Valgus - 10 Newton

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

RADIATIONDevice Valgus - 20 Newton

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

RADIATIONDevice Valgus - 30 Newton

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

RADIATIONDevice Varus - 0 Newton

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

RADIATIONDevice Varus - 10 Newton

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

RADIATIONDevice Varus - 20 Newton

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

RADIATIONDevice Varus - 30 Newton

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

Sponsors

University of Oxford
CollaboratorOTHER
Oxford University Hospitals NHS Trust
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Participants will have the interventions in each of the ten arms of the study.

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Compartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)Day 0Knee minimum joint space width measured on anteroposterior fluoroscopic images using custom, validated, in house software (KneeMorph, MATLAB, MathWorks, Massachusetts).

Secondary

MeasureTime frameDescription
Pain (VAS 0 - 10)At time of procedurePain Score during stress radiographs (VAS 0 - 10) where a higher score represents more pain (10 = worst pain).

Participant flow

Pre-assignment details

In total 9 participants recruited with the interventions in each arm applied to all participants

Participants by arm

ArmCount
All Participants
All participants
9
Total9

Baseline characteristics

CharacteristicAll Participants
Age, Continuous70 years
Region of Enrollment
United Kingdom
9 participants
Sex: Female, Male
Female
9 Participants
Sex: Female, Male
Male
0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
EG004
affected / at risk
EG005
affected / at risk
EG006
affected / at risk
EG007
affected / at risk
EG008
affected / at risk
EG009
affected / at risk
deaths
Total, all-cause mortality
0 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 9
other
Total, other adverse events
0 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 9
serious
Total, serious adverse events
0 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 90 / 9

Outcome results

Primary

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).

Time frame: Day 0

ArmMeasureValue (MEAN)Dispersion
Clinician ValgusCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)7.42 mmStandard Deviation 1.38
Clinician VarusCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)3.92 mmStandard Deviation 2.12
Device Valgus - 0 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)8.22 mmStandard Deviation 1.3
Device Valgus - 10 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)7.47 mmStandard Deviation 1.54
Device Valgus - 20 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)7.31 mmStandard Deviation 1.71
Device Valgus - 30 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)7.33 mmStandard Deviation 1.62
Device Varus - 0 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)8.56 mmStandard Deviation 1.44
Device Varus - 10 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)4.41 mmStandard Deviation 1.83
Device Varus - 20 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)3.7 mmStandard Deviation 2.08
Device Varus - 30 Newton ForceCompartment Specific Knee Minimum Joint Space Width (Varus - Medial Compartment, Valgus - Lateral Compartment)3.84 mmStandard Deviation 2.28
Secondary

Pain (VAS 0 - 10)

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

Time frame: At time of procedure

ArmMeasureValue (MEAN)Dispersion
Clinician ValgusPain (VAS 0 - 10)3.67 units on a scaleStandard Deviation 2.08
Clinician VarusPain (VAS 0 - 10)4.00 units on a scaleStandard Deviation 2
Device Valgus - 0 Newton ForcePain (VAS 0 - 10)0 units on a scaleStandard Deviation 0
Device Valgus - 10 Newton ForcePain (VAS 0 - 10)0.78 units on a scaleStandard Deviation 0.74
Device Valgus - 20 Newton ForcePain (VAS 0 - 10)1.56 units on a scaleStandard Deviation 2.35
Device Valgus - 30 Newton ForcePain (VAS 0 - 10)5.44 units on a scaleStandard Deviation 2.01
Device Varus - 0 Newton ForcePain (VAS 0 - 10)0 units on a scaleStandard Deviation 0
Device Varus - 10 Newton ForcePain (VAS 0 - 10)0.88 units on a scaleStandard Deviation 1.64
Device Varus - 20 Newton ForcePain (VAS 0 - 10)1.25 units on a scaleStandard Deviation 2.31
Device Varus - 30 Newton ForcePain (VAS 0 - 10)4.88 units on a scaleStandard Deviation 1.36

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026