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.
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.
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)
- Conditions
- Knee Osteoarthritis
- 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 group | Role | What they receive |
|---|---|---|
| EM Technique | Experimental | use of extramedullary technique by means of inertial sensors for the execution of femoral cuts Receives: Procedure: Total knee replacement |
| IM Technique | Active comparator | Use 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.
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)
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
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
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
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.
- First posted27 Jan 2020
- Study start18 Sep 2019
- Primary completion26 May 2023
- Study completion26 May 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Knee OsteoarthritisStudies of the same condition, open and under way.
- More trials run by Istituto Ortopedico RizzoliThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Istituto Ortopedico Rizzoli
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Giulio Maria Marcheggiani Muccioli, MD, PhD, Principal investigator, IRCCS Rizzoli Orthopedic Institute
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
Study at a glance
From the registry record, last updated by the sponsor on 31 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT04242303
- Acronym / sponsor ID
- TKA_EM2
- Conditions
- Knee Osteoarthritis
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 180 participants (actual)
- Lead sponsor
- Istituto Ortopedico RizzoliUniversity, hospital or other
- Study start
- 18 Sep 2019 (actual)
- Primary completion
- 26 May 2023 (actual)
- Study completion
- 26 May 2023 (actual)
- First posted
- 27 Jan 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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)
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- 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
| Arm | Type | Receives |
|---|---|---|
| EM Technique | Experimental | Procedure: Total knee replacementuse of extramedullary technique by means of inertial sensors for the execution of femoral cuts |
| IM Technique | Active comparator | Procedure: Total knee replacementUse of conventional intramedullary technique for the execution of femoral cuts |
Who may qualify
- Ages
- 40 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- patients candidated for total knee arthroplasty
- hip mobility range of at least 30 °
- BMI <35kg / m2
- Aged between 40 and 80 years
Key exclusion criteria (4 listed)
- ipsilateral hip arthrodesis or ankylosis
- non-perforable femoral medullary canal
- 165 °<HKA <195 °
- BMI> 35kg / m2
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Total knee replacementTotal 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. | Procedure or surgery | EM Technique, IM Technique |
Primary outcome
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
* 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
4 secondary outcomes
Reduction of the variation in hemoglobin levels during hospitalization.
Time frame: 22 months
Reduction of alignment errors of the femoral and tibial resections obtained with the EM technique and with the IM technique on the sagittal plane
Time frame: 22 months
Reduction of the period of hospital stay in the EM group compared to the group operated with the standard technique
Time frame: 22 months
Inter-operator variability in the EM group
Time frame: 22 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 May 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Giulio Maria Marcheggiani Muccioli, MD, PhD principal investigator
IRCCS Rizzoli Orthopedic Institute
1 site in 1 country: see every site and its status.
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.