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A Prospective Study to Evaluate Robot Assisted Total Knee Replacement Outcomes

NCT03523897 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 92

Last updated 2025-06-06

Study results available
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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

  • Primary Osteoarthritis of Knee Nos

Interventions

PROCEDURE

Robot Assisted Total Knee Replacement

A 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

PROCEDURE

Traditional Total Knee Replacement

A 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

Sponsors & Collaborators

  • Virtua Health, Inc.

    lead OTHER

Principal Investigators

  • Jeremy Reid, MD · Virtua Joint Replacement Institute

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-04-20
Primary Completion
2022-07-14
Completion
2022-07-14

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 NCT03523897 on ClinicalTrials.gov