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NCT03053453 · ClinicalTrials.gov registry record · NA
Evaluation of Patient Reported Outcomes (PRO) After Total Knee Arthroplasty (TKA) Under Spinal Anesthesia
A NA study, sponsored by NYU Langone Health.
- Terminated
- Registry status
- NA
- Development phase
- 52
- Enrollment target
NCT03053453 is a NA study that was terminated before completion, run by NYU Langone Health. The registered enrollment target is 52 participants.
The verdict
NCT03053453, a NA study, was terminated before completion, sponsored by NYU Langone Health.
- TERMINATED
- Registry status
- NA
- Development phase
- 52 participants
- Enrollment target
Study 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.
Interventions
- PROCEDURE Spinal Surgery
- DEVICE Verasense Knee System device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 52 participants |
| Start Date | 2016-12-06 |
| Est. Completion | 2022-07-13 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03053453
The ClinicalTrials.gov registry entry for NCT03053453 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Spinal Surgery is the first listed.
NCT03053453 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03053453 about?
NCT03053453 is a clinical study titled "Evaluation of Patient Reported Outcomes (PRO) After Total Knee Arthroplasty (TKA) Under Spinal Anesthesia". 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 pressu...
What is the current status of trial NCT03053453?
This trial is currently terminated. It is a NA study. The enrollment target is 52 participants. The study started on 2016-12-06. Estimated completion is 2022-07-13.
What interventions are being tested in trial NCT03053453?
The interventions under investigation include: Spinal Surgery (PROCEDURE), Verasense Knee System device (DEVICE).
Who is sponsoring clinical trial NCT03053453?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
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