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ArthroplastyNCT06527911

A Randomized Controlled Trial of the Sagittal Alignment Difference Between Mako Robotic TKA and Manual TKA

An observational study of Arthroplasty and Replacement, run by Chinese PLA General Hospital at 1 site in China.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

As China transitions into an aging society, the proportion of the elderly population is escalating, with a corresponding rise in the number of patients with knee joint diseases. Total knee arthroplasty stands as an effective treatment for joint disorders, effectively reducing knee pain, restoring functionality, and… Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Arthroplasty, Replacement, Knee
How many people
100 participants
Where
1 siteChina
Study dates
1 Sep 2024to 1 Sep 2026
How long will I take part?
3 Years
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 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: OA patients who underwent Mako robot assisted TKA and manual TKA (Stryker Triathlon prosthesis) in the Department of joint surgery of the PLA General Hospital from September 2024 to September 2026 were screened.

Who may be able to join

  • The age ranged from 18 to 80 years old;
  • OA patients who underwent Mako robot assisted TKA and manual TKA (Stryker Triathlon prosthesis) in the Department of joint surgery of the PLA General Hospital from September 2024 to September 2026;
  • All patients were required to take full-length anteroposterior and lateral radiographs of lower limbs, anteroposterior and lateral radiographs of both knees, and lower limb sagittal EOS before and after surgery;
  • Physical and mental health, able to participate in and cooperate with the test;
  • Patients are willing to participate in the study and sign written informed consent.

Who cannot join

  • People unable to conduct EOS inspection;
  • Combined with knee meniscus injury, anterior cruciate ligament injury and other diseases that may affect the sagittal force line of the knee joint
  • Combined with other diseases that may affect the study
  • Patients refused to use their imaging data and knee score for this study.

Trial locations and contacts

1 site in 1 country.

Wei Chai, doctorate contact

13601372998

chaiwei301@163.com

China1 site
  • Chinese PLA General Hospital

    Beijing, Beijing Municipality, 100037

Other trials in China

About this study

Official title: A Randomized Controlled Trial of the Sagittal Alignment Difference Between Mako Robotic Total Knee Arthroplasty and Manual Total Knee Arthroplasty

As China transitions into an aging society, the proportion of the elderly population is escalating, with a corresponding rise in the number of patients with knee joint diseases. Total knee arthroplasty stands as an effective treatment for joint disorders, effectively reducing knee pain, restoring functionality, and enhancing quality of life. The objectives of total knee arthroplasty are to relieve pain, restore function, and ensure a long-lasting implant. In recent years, technological advancements have integrated robotic assistance into total knee arthroplasty (TKA), aiding surgeons in planning and executing more accurate surgical plans, significantly enhancing precision and post-operative outcomes. However, the Mako mechanical axis alignment demonstrated during the Mako robot-assisted TKA procedure does not correspond to the actual straightening of the lower limb, and discrepancies may exist in sagittal alignment between Mako-assisted and manual TKA procedures, necessitating adjustments by surgeons based on their experience. Consequently, there is an urgent need to develop a mathematical formula that quantifies these differences to guide intraoperative alignment. Additionally, the Mako-assisted TKA femoral prosthesis exhibits a head-lowering issue, and differences exist in the posterior slope angle of the tibial plateau compared to manual TKA, necessitating further comparative analysis to draw definitive conclusions. This study will be carried out at the People's Liberation Army General Hospital, with an anticipated enrollment of approximately 100 participants.

Read the detailed description
  1. Clinical Research Background As China transitions into an aging society, the proportion of the elderly population is escalating, with a corresponding rise in the number of patients with knee joint diseases. Total knee arthroplasty stands as an effective treatment for joint disorders, effectively reducing knee pain, restoring functionality, and enhancing quality of life. The objectives of total knee arthroplasty are to relieve pain, restore function, and ensure a long-lasting implant. In recent years, technological advancements have integrated robotic assistance into total knee arthroplasty (TKA), aiding surgeons in planning and executing more accurate surgical plans, significantly enhancing precision and post-operative outcomes. However, the Mako mechanical axis alignment demonstrated during the Mako robot-assisted TKA procedure does not correspond to the actual straightening of the lower limb, and discrepancies may exist in sagittal alignment between Mako-assisted and manual TKA procedures, necessitating adjustments by surgeons based on their experience. Consequently, there is an urgent need to develop a mathematical formula that quantifies these differences to guide intraoperative alignment. Additionally, the Mako-assisted TKA femoral prosthesis exhibits a head-lowering issue, and differences exist in the posterior slope angle of the tibial plateau compared to manual TKA, necessitating further comparative analysis to draw definitive conclusions.

II. Content of Clinical Trials (I) Overall Design and Sample Size This study is a prospective clinical investigation, encompassing two groups: ① the Mako robot-assisted TKA group: patients with osteoarthritis (OA) who underwent Mako robot-assisted TKA at the Chinese PLA General Hospital between September 2024 and September 2026; and ② the manual TKA group: patients with OA who underwent manual TKA at the same hospital between September 2024 and September 2026.

(II) Randomization and Control in the Trial Randomized Controlled Trial (III) Content This clinical study aims to compare the differences between the extension demonstrated during Mako robot-assisted TKA surgery and the actual postoperative extension, proposing a mathematical formula to reflect these discrepancies. Through the validation of intraoperative and postoperative data, the study aims to guide the extension during Mako-assisted TKA. Additionally, In Mako-assisted TKA, there is a femoral prosthesis bowing down issue, and the posterior inclination angle of the tibial plateau differs from that of manual TKA. Consequently, the sagittal femoral bowing down angle and posterior inclination angle of the tibial plateau were compared between robot-assisted TKA and manual TKA to verify the differences between the groups.This study was conducted at the Joint Surgery Department of the Chinese PLA General Hospital, with participants meeting inclusion criteria and not violating exclusion criteria, and having signed informed consent forms approved by the ethics committee.

III: Trial Procedure (I) Participant Enrollment Physicians selected osteoarthritis (OA) patients who underwent total knee arthroplasty (TKA) at our hospital from September 2024 to September 2026, and screened them based on inclusion and exclusion criteria. If a patient met the inclusion criteria, the details of the research project were thoroughly explained to them, and they were required to sign the relevant informed consent form.

(II) Methodology A clinical study was conducted at the Joint Surgery Department of the Chinese PLA General Hospital from September 2024 to September 2026, involving 50 patients each undergoing Mako robot-assisted TKA and manual TKA (Stryker Triathlon prosthesis). Basic patient information, including ID number, name, gender, age, height, and weight, was recorded. Preoperative and postoperative full-length lateral radiographs of the lower limbs, bilateral knee joint lateral radiographs, and sagittal EOS of the lower limbs were taken for all patients. An experienced researcher measured the posterior slope angle of the tibial plateau preoperatively and postoperatively using the Mako robot-assisted TKA, as well as the extension angle displayed by the Mako at the end of the TKA procedure. Based on the differences preoperatively and postoperatively in the 50 cases of Mako robot-assisted TKA, a mathematical formula reflecting extension was proposed and validated. Preoperative and postoperative coronal HKA, LDFA, and MPTA measurements were taken for both Mako robot-assisted TKA and manual TKA; preoperative and postoperative sagittal measurements of the posterior slope angle of the tibial plateau; and postoperative femoral prosthesis head tilt angle were recorded, and statistical analysis was conducted to compare the sagittal angle differences between Mako robot-assisted and manual TKA.

(III) Clinical Evaluation Indices (1) Primary Outcome Measures:

  1. The extension angle displayed by the Mako robot at the conclusion of the Mako-assisted Total Knee Arthroplasty (TKA) procedure;
  2. Sagittal plane femoral anterior arch angle;
  3. Preoperative and postoperative coronal hip-knee-ankle (HKA) angles, lateral distal femoral angle (LDFA), and medial proximal tibial angle (MPTA) in Mako robot-assisted TKA and manual TKA;
  4. Preoperative and postoperative sagittal measurement of the tibial plateau posterior slope angle; postoperative femoral prosthesis head-down angle. (2) Secondary Observational Indicators
  5. Basic demographic data of the patients.
  • Statistical Analysis Methods All results were computed using SPSS 26.0. A comprehensive enumeration of the collected data will be presented, followed by a descriptive summary of the data. Categorical variables will be summarized using frequencies and percentages, while continuous variables will be summarized by the number of subjects at each evaluation time point, mean values, mean differences relative to baseline values (where appropriate), medians, standard deviations, 95% confidence intervals, minimum values, and maximum values.

Prior to database lock, the definitive statistical analysis plan will be established, and the pertinent clinical and statistical personnel will document their decisions regarding the inclusion or exclusion of data from each subject.

Medical subject headings
Osteoarthritis

What participants receive

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

Study groups in NCT06527911
Study groupRoleWhat they receive
Mako robot assisted TKAPatients with osteoarthritis (OA) who underwent Mako robot-assisted TKA at the Chinese PLA General Hospital between September 2024 and September 2026.
Manual TKAPatients with OA who underwent manual TKA at the Chinese PLA General Hospital between September 2024 and September 2026.

What is being measured

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

  1. The extension angle displayed by the Mako robot at the conclusion of the Mako-assisted Total Knee Arthroplasty (TKA) procedure

    Measured: From admission to discharge, up to 1 week

  2. Sagittal plane femoral anterior arch angle

    Measured: From admission to discharge, up to 1 week

  3. Preoperative and postoperative coronal hip-knee-ankle (HKA) angles, lateral distal femoral angle (LDFA), and medial proximal tibial angle (MPTA) in Mako robot-assisted TKA and manual TKA

    Measured: From admission to discharge, up to 1 week

  4. Preoperative and postoperative sagittal measurement of the tibial plateau posterior slope angle; postoperative femoral prosthesis head-down angle

    Measured: From admission to discharge, up to 1 week

Secondary outcomes (1)
  1. Basic demographic profile of the patient

    Measured: From admission to discharge, up to 1 week

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 2024
  2. Study start1 Sep 2024 (estimated)
  3. Primary completion1 Sep 2025 (estimated)
  4. Study completion1 Sep 2026 (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
100 participants (estimated)
Target duration
3 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT06527911
Sponsor's protocol ID
2023KY023-KS001
Status last verified
Jul 2024
First submitted
25 Jul 2024
Last updated
30 Jul 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Arthroplasty and Replacement, run by Chinese PLA General Hospital at 1 site in China.

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 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: status not confirmed, as of the sponsor's last update on 30 Jul 2024. 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 China. 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?

Contact Wei Chai, doctorate (13601372998, chaiwei301@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The extension angle displayed by the Mako robot at the conclusion of the Mako-assisted Total Knee Arthroplasty (TKA) procedure (time frame: From admission to discharge, up to 1 week). The study lists 4 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 30 Jul 2024.

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