Trials / Terminated
TerminatedNCT03053453
Evaluation of Patient Reported Outcomes (PRO) After Total Knee Arthroplasty (TKA) Under Spinal Anesthesia
Evaluation of the Patient Reported Outcomes After Sensor-guided Total Knee Arthroplasty Under Spinal Anesthesia With Limited Motor-block.
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 52 (actual)
- Sponsor
- NYU Langone Health · Academic / Other
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study will be to evaluate and compare patients undergoing total knee arthroplasty (TKA) with sensor guidance versus that of a standard technique. Each patient will be assessed for the difference between passive, soft tissue controlled, pressure balance and muscle activated pressure balance.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Spinal Surgery | TKA under standard of care spinal surgery. |
| DEVICE | Verasense Knee System device | Sensor measures and localizes peak load at the medial and lateral tibiofemoral joint interfaces. Loading data is thereby captured intra-operatively through the full range of movement (ROM) using the sensor system. |
Timeline
- Start date
- 2016-12-06
- Primary completion
- 2022-07-13
- Completion
- 2022-07-13
- First posted
- 2017-02-15
- Last updated
- 2023-11-14
- Results posted
- 2023-11-14
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03053453. Inclusion in this directory is not an endorsement.