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NCT03088748 · ClinicalTrials.gov registry record
Kinematics in Posterior Cruciate Retaining and Bi-Cruciate Retaining Total Knee Replacements
A clinical trial, sponsored by The University of Tennessee, Knoxville.
- Completed
- Registry status
- 50
- Enrollment target
NCT03088748: Completed study, sponsored by The University of Tennessee, Knoxville.
NCT03088748 is a clinical trial that has completed, run by The University of Tennessee, Knoxville. The registered enrollment target is 50 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03088748 has completed, sponsored by The University of Tennessee, Knoxville.
- COMPLETED
- Registry status
- 50 participants
- Enrollment target
Study Summary
The purpose of the study is to acquire kinematic in vivo fluoroscopy data from subjects who were implanted with the Smith \& Nephew Journey II posterior cruciate retaining (PCR) total knee arthroplasty (TKA) or Journey II bi-cruciate retaining (BCR) TKA. CMR has previously collected data for the Smith \& Nephew BCS TKA and compared these kinematics data to those of normal knees.
Primary Outcome
Anterior Posterior (AP) translations of lateral femoral condyles during activity of walking up a ramp. Data represents the motion of a specific part of the femur bone (in this case lateral femoral condyle) during the specified activity (in this case a ramp up). The kinematics (motion) is measured from the beginning of the activity to the end of the activity. Positive represents anterior motion of the femur, and negative represents posterior rollback of the femur. Data is only collected at a sing
Interventions
- DEVICE Journey II posterior cruciate retaining total knee arthroplasty
- DEVICE Journey II posterior bi-cruciate retaining total knee arthroplasty
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2017-01 |
| Est. Completion | 2020-11-09 |
What the finished NCT03088748 record still lists
NCT03088748 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target.
The record links to 0 conditions, and to 2 interventions - of which Journey II posterior cruciate retaining total knee arthroplasty is the first listed.
NCT03088748 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03088748 about?
NCT03088748 is a clinical study titled "Kinematics in Posterior Cruciate Retaining and Bi-Cruciate Retaining Total Knee Replacements". The purpose of the study is to acquire kinematic in vivo fluoroscopy data from subjects who were implanted with the Smith \& Nephew Journey II posterior cruciate retaining (PCR) total knee arthroplasty (TKA) or Journey II bi-cruciate retaining (BCR) TKA. CMR has previously collected data for the Smi...
What is the current status of trial NCT03088748?
This trial is currently completed. The enrollment target is 50 participants. The study started on 2017-01. Estimated completion is 2020-11-09.
What interventions are being tested in trial NCT03088748?
The interventions under investigation include: Journey II posterior cruciate retaining total knee arthroplasty (DEVICE), Journey II posterior bi-cruciate retaining total knee arthroplasty (DEVICE).
Who is sponsoring clinical trial NCT03088748?
This trial is sponsored by The University of Tennessee, Knoxville, which has 81 total clinical trials registered on ClinicalTrials.gov.
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