Osteoarthritis, Knee Clinical Trial
Official title:
Outcomes in Free-hand Versus Sensor-guided Balancing in Total Knee Arthroplasty: a Randomized Controlled Trial
Verified date | September 2021 |
Source | Columbia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In a randomized-controlled fashion, this investigation will evaluate the use of the Verasense technology to achieve optimal TKA balance. Patients will be randomized to either: 1) undergo manual soft tissue balancing or 2) soft tissue balancing with the Verasense. The primary outcomes of interest will include patient-reported outcomes as well knee range of motion at 3 months, 6 months, 1 year, and 2 years. Secondary outcomes of interest will include pain level as assessed by the visual analogue scale (VAS) in the acute post-operative and follow up periods, ambulation distance during inpatient physical therapy postoperatively, surgical time, tourniquet time, amount of opioid consumption, length of hospital stay, incidence of arthrofibrosis and subsequent manipulation under anesthesia. The investigators hypothesize that the use of the Verasense technology will lead to improved soft tissue balancing in TKA and ultimately result in favorable patient-reported outcomes and postoperative knee range of motion.
Status | Active, not recruiting |
Enrollment | 130 |
Est. completion date | December 20, 2022 |
Est. primary completion date | September 20, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility | Inclusion Criteria: - Primary total knee replacement Exclusion Criteria: - Revision knee surgery - Prior knee surgery |
Country | Name | City | State |
---|---|---|---|
United States | NewYork-Presbyterian Lawrence Hospital | Bronxville | New York |
United States | Columbia University Medical Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University |
United States,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Veterans RAND12 Item Health Survey | The investigators will ask participants to answer survey questions about knee functionality on a scale of 0-100, 0 being the least functionality and 100 being the most. | 1 year | |
Secondary | Visual Analogue Scale pain level | Pain levels on a scale from 1-10 (1 being the least amount of pain possible and 10 being the most amount of pain possible). | 1 week | |
Secondary | Ambulation (distance) | ambulation distance during inpatient physical therapy postoperatively | 1 week | |
Secondary | Range of motion | physical examination of knee | 1 year | |
Secondary | KOOS Knee Survey | The investigators will ask participants to answer survey questions about knee functionality on a scale of 0-100, 0 being the least functionality and 100 being the most. | 1 year |
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