AzTrials
AzTrials

Knee OsteoarthritisNCT04242303

Effectiveness of Inertial Sensors vs the Conventional Technique for the Execution of the Bone Resections in Primary TKA

A study testing Total knee replacement in people with Knee Osteoarthritis, run by Istituto Ortopedico Rizzoli at 1 site in Italy.

Completed

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

Official record
Search all trials

Trial summary

Comparison of surgical technique for the execution of bone resections in total knee arthroplasty. Used technique are: a non-invasive extramedullary technique (EM technique) based on the use of inertial sensors for cutting guides positioning and conventional technique (IM technique), based on the use on intramedullary… Read more about this study

Who is it for?
Ages 40 to 80 years
Conditions the study is for
Knee Osteoarthritis
What is being tested?
Total knee replacement
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
180 participants
Where
1 siteItaly
Study dates
18 Sep 2019to 26 May 2023
Phase
Interventional
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 40 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • patients candidated for total knee arthroplasty
  • hip mobility range of at least 30 °
  • BMI <35kg / m2
  • Aged between 40 and 80 years

Who cannot join

  • ipsilateral hip arthrodesis or ankylosis
  • non-perforable femoral medullary canal
  • 165 °<HKA <195 °
  • BMI> 35kg / m2

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • IRCCS Istituto Ortopedico Rizzoli

    Bologna, 40136

Other trials in Italy

About this study

Official title: Evaluation of the Effectiveness of a Technique Based on Inertial Sensors vs the Conventional Technique for the Execution of the Bone Resections in Primary Total Knee Arthroplasty: a Controlled Randomized Trial

Comparison of surgical technique for the execution of bone resections in total knee arthroplasty.

Used technique are: a non-invasive extramedullary technique (EM technique) based on the use of inertial sensors for cutting guides positioning and conventional technique (IM technique), based on the use on intramedullary stem.

Our hypothesis is that the EM technique based on the use of inertial sensors leads to a reduction in the number of outliers equal to or greater than 20% compared to the outliers obtained with the conventional technique.

Read the detailed description

Comparison of surgical technique for the execution of bone resections in total knee arthroplasty.

Used technique are: a non-invasive extramedullary technique (EM technique) based on the use of inertial sensors for cutting guides positioning and conventional technique (IM technique), based on the use on intramedullary stem. A study was carried out at the Rizzoli Orthopedic Institute in 2016 to compare non-invasive extramedullary technique (EM technique) and conventional technique (IM technique). Starting from the results obtained in the previous study, the objective of this study is to deepen the investigations to evaluate the effectiveness of the EM technique compared to the conventional IM technique.

The patients involved in the study will be divided into two groups based on the alignment technique used (EM technique and IM technique).

The results obtained will be measured on postoperative panoramic radiographs at discharge, assessing the overall alignment of the limb and the individual femoral and tibial components in terms of accuracy and repeatability according to a defined measurement protocol.

Primary endpoint:

  • reduction in the number of cases in which the alignment error on the coronal plane is greater than 3°of error (outlier). Our hypothesis is that the EM technique based on the use of inertial sensors leads to a reduction in the number of outliers equal to or greater than 20% compared to the outliers obtained with the conventional technique.

Secondary endpoints:

  • the reduction of the variation in hemoglobin levels during hospitalization. Our hypothesis is that the EM technique leads to a reduction in the maximum variation of hemoglobin levels during the hospitalization period compared to the IM technique equal to or greater than 1g / dl
  • reduction of alignment errors of the femoral and tibial resections obtained with the EM technique and with the IM technique on the sagittal plane. In particular, the experimental hypothesis is that in the EM technique group, values of alignment of the implant with respect to the femoral and tibial mechanical axis on the sagittal plane are not significantly lower than those obtained with the standard technique but with a reduction in the standard deviation in the EM group compared to the IM group.
  • reduction of the period of hospital stay in the EM group compared to the group operated with the standard technique.
  • inter-operator variability in the EM group Randomized controlled multicenter prospective study. The evaluation of the results obtained will be blinded by an examiner with adequate clinical skills and who does not take part in the operational phases of the study.

Duration: 36 months The patients will be divided into 2 groups, based on the alignment technique used Total number of patients involved: 180 (90 Group A Patients: EM Technique), (90 Group B Patients: IM Technique) Total number of centers involved: 3 Patients per Center: 30 Group A Patients, 30 Group B Patients Patients will be randomized. The randomization list will be generated using the website www.randomization.com. This list will be kept at the Operative Unit Orthopedic and Traumatological Clinic 2nd and will not be visible to the investigators involved The evaluation of the results obtained will be carried out blindly by an examiner with adequate clinical skills to carry out the evaluation and who does not take part in the operational phases of the study.

For both groups of patients, the results obtained will be measured on postoperative panoramic radiographs performed at discharge, assessing in terms of accuracy and repeatability.

Finally, within Group A, the inter-operator variability of the measurement of the final femoral and tibial alignment obtained using the Blant \& Altman analysis method will be assessed

The study involves the collection of data in three different phases:

Preoperative phase:

  • Panoramic radiography under weight-bearing of the lower limbs in A-P and radiography of the knee in lateral projection
  • laboratory value of hemoglobin

Intraoperative phase:

  • Time of application of the ischemic snare;
  • Surgery time;
  • Final femoral and tibial alignment. In Group A the acquisition is repeated 2 times by two operators.
  • Number of repetitions of distal femoral and tibial resections;
  • Possible administration of blood products;
  • Blood loss;

Post-operative phase

  • Panoramic X-ray under weight-bearing of the lower limbs in A-P and knee radiography in lateral projection (at discharge)
  • laboratory value of the patient's hemoglobin on each day until the date of discharge
  • possible administration of blood products
  • hospitalization times All data will be collected in a data collection form associated with the patient.

The preoperative and postoperative radiographs (made anonymous) and the data collection form will be sent to the coordinating center which will carry out the measurements.

From the literature it emerges that in order to detect a difference between the two techniques of 20% on the number of outliers (alignment of the components >±3°on the coronal plane) with an alpha type error (level of significance) equal to 0.05 and a power of at least 0.8, the minimum number of samples needed per group is 82 cases. Considering a 10% drop out, a sample of 90 cases per group is expected (divided into 3 centers for a total of 30 cases per group in each center)

Being tested
Total knee replacement
Medical subject headings
Osteoarthritis, Knee

What participants receive

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

  • Total knee replacementProcedure or surgery

    Total knee arthroplasty using standard anterior approach. In the EM group, inertial sensor will be used to perform femoral bone cuts.

    In the IM group, conventional intramedullary nail will be used as reference to perform femoral bone cuts.

Study groups in NCT04242303
Study groupRoleWhat they receive
EM TechniqueExperimentaluse of extramedullary technique by means of inertial sensors for the execution of femoral cuts
Receives: Procedure: Total knee replacement
IM TechniqueActive comparatorUse of conventional intramedullary technique for the execution of femoral cuts
Receives: Procedure: Total knee replacement

What is being measured

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

  1. Reduction in the number of cases in which the alignment error on the coronal plane is greater than 3°of error (outlier).

    • HKA alignment on the coronal plane (medial angle between the femoral mechanical axis and the tibial mechanical axis)
    • coronal femoral angle (medial angle between the femoral mechanical axis and the tangent to the distal condyles of the femoral prosthetic component
    • tibial coronal angle (medial angle between the tibial mechanical axis and the tangent to the proximal profile of the tibial component) The number of patients with an HKA angle such that 180°-3°> HKA> 180°+ 3°or 180°-2°> HKA> 180°+ 2°will also be evaluated

    Measured: 22 months

Secondary outcomes (4)
  1. Reduction of the variation in hemoglobin levels during hospitalization.

    The maximum variation of hemoglobin during the period of hospitalization will also be assessed within each group by comparing the hemoglobin value at the time of hospitalization with the hemoglobin values during the post-operative hospital stay

    Measured: 22 months

  2. Reduction of alignment errors of the femoral and tibial resections obtained with the EM technique and with the IM technique on the sagittal plane

    Sagittal femoral angle (angle between the mechanical femoral axis on the sagittal plane and the distal femoral resection plane) Tibial slope (angle between the tibial mechanical axis on the sagittal plane and the tangent to the proximal profile of the tibial component)

    Measured: 22 months

  3. Reduction of the period of hospital stay in the EM group compared to the group operated with the standard technique

    Hospital stay will be measured in day of hospitalization

    Measured: 22 months

  4. Inter-operator variability in the EM group

    The inter-operator variability of the measurement of the final femoral and tibial alignment obtained using the Blant \& Altman analysis method will be assessed

    Measured: 22 months

Timeline

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

  1. First posted27 Jan 2020
  2. Study start18 Sep 2019
  3. Primary completion26 May 2023
  4. Study completion26 May 2023

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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
The patients will be divided into 2 groups, based on the alignment technique used Total number of patients involved: 180 (90 Group A Patients: EM Technique), (90 Group B Patients: IM Technique) Total number of centers involved: 3 Patients per Center: 30 Group A Patients, 30 Group B Patients
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
180 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04242303
Sponsor's protocol ID
TKA_EM2
Status last verified
May 2023
First submitted
20 Jan 2020
Last updated
31 May 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Total knee replacement in people with Knee Osteoarthritis, run by Istituto Ortopedico Rizzoli at 1 site in Italy.

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 4 inclusion and 4 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 31 May 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 Italy. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Reduction in the number of cases in which the alignment error on the coronal plane is greater than 3°of error (outlier). (time frame: 22 months). 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 31 May 2023.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in
Clinical Trial NCT04242303 | AzTrials