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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 is a clinical trial that has completed, run by The University of Tennessee, Knoxville. The registered enrollment target is 50 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03088748
The ClinicalTrials.gov registry entry for NCT03088748 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Tennessee, Knoxville, which has 81 total studies on file at ClinicalTrials.gov.
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 reports 0 study locations.
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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