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Clinical Trial Summary

This study aims to see if outcomes for patients that receive the traditional total knee replacement surgical technique are different than the outcomes for patients that receive robot-assisted total knee replacement. The outcomes we will be tracking include: 1. Patients' self-reported awareness of their artificial joints during activities of daily living; 2. Patient's self-reported pain, other symptoms, function in daily living, function in sport and recreation, and knee-related quality of life; 3. Patients' self-reported general health perceptions, physical functioning, role limitations due to physical and emotional problems, bodily pain, energy-fatigue, social functioning and mental health; 4. The accuracy of implant placement and limb alignment


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03523897
Study type Interventional
Source Virtua Health, Inc.
Contact Jeremy K Reid, MD
Phone 917-763-6790
Email jreid@reconstructiveortho.com
Status Recruiting
Phase N/A
Start date April 20, 2018
Completion date December 31, 2023

See also
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Completed NCT04998825 - Efficacy and Tolerability of Proteoglycan F in the Treatment of Knee Osteoarthritis N/A
Completed NCT03232957 - Intrathecal Morphine for Unilateral Total Knee Arthroplasty N/A
Recruiting NCT05509972 - In-vivo Wear Behaviour of AS Coated Versus Uncoated Columbus® Total Knee Prosthesis