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Verasense Knee System device for Knee Injuries

N/A
Waitlist Available
Led By Arthur Hertling, MD
Research Sponsored by NYU Langone Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up month 12 post-surgery
Awards & highlights

Study Summary

This trial will compare two methods of performing total knee arthroplasty, one with sensor guidance and one without. The goal is to see if the sensor-guided method leads to better outcomes.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~month 12 post-surgery
This trial's timeline: 3 weeks for screening, Varies for treatment, and month 12 post-surgery for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Knee
Knee Society Score (KSS)

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Sensor Guided Spinal SurgeryExperimental Treatment1 Intervention
The Verasense Knee System device (OrthoSensor inc., Dania Beach, Florida) is a sterile sensor system that replaces the tibial insert trials used during surgery. The sensor contains a microprocessor and integrated nanosensor system, which wirelessly transmits real-time data to a portable graphic display unit used for read-out of the data. The sensor measures and localizes peak load at the medial and lateral tibiofemoral joint interfaces. Loading data is thereby captured intra-operatively through the full range of movement (ROM) using the sensor system.
Group II: Standard of Care Spinal SurgeryActive Control1 Intervention
Patients will be given spinal anesthesia with 2.6 mL of 0.5% isobaric bupivacaine.

Find a Location

Who is running the clinical trial?

NYU Langone HealthLead Sponsor
1,368 Previous Clinical Trials
839,674 Total Patients Enrolled
Arthur Hertling, MDPrincipal InvestigatorNYU Langone Health
3 Previous Clinical Trials
196 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Evaluation of Patient Reported Outcomes (PRO) After Total Knee Arthroplasty (TKA) Under Spinal Anesthesia
2016. "Evaluation of Patient Reported Outcomes (PRO) After Total Knee Arthroplasty (TKA) Under Spinal Anesthesia". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03053453.
~6 spots leftby Apr 2025
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