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

Status unconfirmed · Not applicable

Conditions studied: Arthroplasty, Replacement, Knee

In brief

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.

Key facts

Study ID

NCT02717299

Run by

TriHealth Inc.

People needed

78

Starts

2015-11-01

Expected to finish

2021-04-08

Last updated by the study team

2020-05-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients undergoing primary unilateral total knee arthroplasty for osteoarthritis, avascular necrosis, inflammatory arthropathy, or post traumatic arthritis.
• Patients able to understand study intent, and agree to study participation.
• Patients receiving Smith and Nephew Journey II total knee implant system.

You may not qualify if…

• Patients with previous ipsilateral knee ligament surgery.
• Patients with orthopaedic and medical co-morbidities that would thwart postoperative recovery such as extra-articular pathology with referred pain to the knee (spinal stenosis, neuropathy, ipsilateral hip disease), severe knee deformity.
• Untreated Osteoarthritis
• BMI > 40
• ASA class > III
• History of drug or alcohol abuse

Where it is running

• Good Samarian Hospital — Cincinnati, Ohio, United States

Full record on ClinicalTrials.gov

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