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Making Sense Out of Total Knee Sensor Assisted Technology: A Randomized Control Trial

NCT02717299 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2020-05-04

No results posted yet for this study

Summary

The purpose of this study is to compare the patient reported outcome measures of total knee replacement patients who received intra operative sensor guided technique for soft tissue balancing to a group of patients who receive surgeon guided soft tissue balancing.

Conditions

  • Arthroplasty, Replacement, Knee

Interventions

DEVICE

Verasense

Verasense will collect balancing data on all patients in this trial.

Sponsors & Collaborators

  • Orthosensor, Inc.

    collaborator INDUSTRY

  • TriHealth Inc.

    lead OTHER

Principal Investigators

  • Mark Snyder, MD · TriHealth Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2019-04-30
Completion
2021-04-08

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02717299 on ClinicalTrials.gov