Clinical Trials Directory

Trials / Terminated

TerminatedNCT03523897

A Prospective Study to Evaluate Robot Assisted Total Knee Replacement Outcomes

A Prospective Study to Examine Patient Satisfaction, Function, and Limb Alignment Outcomes for Mako Versus Non-Mako Total Knee Replacements

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
92 (actual)
Sponsor
Virtua Health, Inc. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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

Conditions

Interventions

TypeNameDescription
PROCEDURERobot Assisted Total Knee ReplacementA robotic-assisted surgical procedure to treat a condition in which the patient's knee joints become diseased or injured due to a loss of cartilage that acts as a protective cushion between the knee joints
PROCEDURETraditional Total Knee ReplacementA surgical procedure using mechanical guides to treat a condition in which the patient's knee joints become diseased or injured due to a loss of cartilage that acts as a protective cushion between the knee joints

Timeline

Start date
2018-04-20
Primary completion
2022-07-14
Completion
2022-07-14
First posted
2018-05-14
Last updated
2025-06-06
Results posted
2025-06-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03523897. Inclusion in this directory is not an endorsement.