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NCT02821325 · ClinicalTrials.gov registry record
Intra-articular Volumetric Assessment After Total Knee Arthroplasty
A clinical trial, sponsored by Loma Linda University.
- Completed
- Registry status
- 10
- Enrollment target
NCT02821325: Completed study, sponsored by Loma Linda University.
NCT02821325 is a clinical trial that has completed, run by Loma Linda University. The registered enrollment target is 10 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02821325 has completed, sponsored by Loma Linda University.
- COMPLETED
- Registry status
- 10 participants
- Enrollment target
Study Summary
The purpose of the study: is to quantify the amount of post-operative effusion or hematoma present after total knee arthroplasty pre-operatively, post-operative day #0,1. Patients undergoing a total knee arthroplasty will undergo an MRI on the operative knee at the following times: * Pre-operatively * Post-operative day #1 (approximately 16-20 hours post op) * Post-operative day #2 (approximately 36-40 hours post op) This will be conducted by the Loma Linda radiology department as per normal protocols. No special imaging procedures will be undertaken. Subjects will be both male and females, they will be patients from the Principle Investigator and Co-Investigators practice. Subjects will be between the ages of 18-89 years of age. The total participation will last approximately 30 days. Subject selection will be approximately 10 English speaking, both male and female between the ages of 18 to 89 years of age. Subjects will be recruited from the Principal Investigators and Co-Investigators clinic. There will be no advertising or electronic recruiting. The study is expected to last 12 months.
Primary Outcome
MRI studies will be reviewed on these participants pre-operatively and postoperatively. Data will be analyzed using the Statistical package for social sciences (SPSS) software and paired T-Test will be utilized for significance regarding the effusion post operatively.
Interventions
- OTHER MRI
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2016-09-28 |
| Est. Completion | 2018-01-30 |
What the finished NCT02821325 record still lists
NCT02821325 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 10 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which MRI is the first listed.
NCT02821325 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02821325 about?
NCT02821325 is a clinical study titled "Intra-articular Volumetric Assessment After Total Knee Arthroplasty". The purpose of the study: is to quantify the amount of post-operative effusion or hematoma present after total knee arthroplasty pre-operatively, post-operative day #0,1. Patients undergoing a total knee arthroplasty will undergo an MRI on the operative knee at the following times: * Pre-operative...
What is the current status of trial NCT02821325?
This trial is currently completed. The enrollment target is 10 participants. The study started on 2016-09-28. Estimated completion is 2018-01-30.
What interventions are being tested in trial NCT02821325?
The interventions under investigation include: MRI (OTHER).
Who is sponsoring clinical trial NCT02821325?
This trial is sponsored by Loma Linda University, which has 237 total clinical trials registered on ClinicalTrials.gov.
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