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Clinical Trials in Canada / NCT01674816
Starting soon Not applicable

Minimally Invasive Three-dimensional Knee Kinematic Assessment and Surgical Guidance Using Ultrasonic Rigid Registration

NCT01674816 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-12-01
Last updated
2024-02-12

Condition(s) studied

Knee OsteoarthritisKnee Instability3D Knee KinematicsPrecision of Surgical ActionsClinical Outcomes

Investigational drug(s) / intervention(s)

Repeated Measurements of Knee Alignment and KinematicsComputer Guidance of Surgical Actions

Repeated Measurements of Knee Alignment and Kinematics: Repeated Measurements of Knee Alignment and Kinematics using tools developed by Eiffel Medtech Inc.

Computer Guidance of Surgical Actions: Computer Guidance of Surgical Actions using tools developed by Eiffel Medtech Inc.

Study summary

Problem:

Currently, no system allows precise kinematic assessment of the knee and accurate guiding of orthopedic surgical actions in a minimally invasive fashion. However, such a system would prove useful in the clinical setting to improve the quality of surgical interventions at the knee.

Hypothesis:

A novel knee kinematic assessment and surgical guidance tool using 3D personalized imaging and minimally invasive bony fixation allows precise kinematic assessment and surgical guidance in the routine clinical setting.

Objectives :

* Demonstrating the capacity of the system to precisely measure 3D knee kinematics
* Quantifying the reproducibility of the kinematic measurements
* Measuring the impact of knee surgical procedures on knee kinematics
* Assessing the correlations between measured articular kinematics and clinical results after knee surgery
* Integrating the novel measuring system to the surgical flow of three knee surgical procedures
* Quantifying the precision and reproducibility of the surgical actions guided by the system
* Comparing the clinical results of surgeries guided by the system to those performed with the traditional technique

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients awaiting a knee surgery (total knee arthroplasty (TKA), high tibial osteotomy (HTO), anterior cruciate ligament reconstruction(ACLR)) Exclusion Criteria: * Active infection * Atypical morphology and/or alignment of the lower limbs * Knee instability (other than secondary to ACL deficiency in patients awaiting ACLR) * Knee flexion contracture of 10 degrees or more * Knee flexion of less than 120 degrees

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre Hospitalier de l'Université de Montréal (CHUM) Montreal Quebec

More Centre hospitalier de l'Université de Montréal (CHUM) trials in Canada

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01674816 on ClinicalTrials.gov ↗ ← All trials in Canada