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NCT02219087 · ClinicalTrials.gov registry record · NA
Liposomal Bupivacaine Versus Standard of Care in Total Knee Surgery
A NA study, sponsored by OhioHealth.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT02219087: Completed NA study, sponsored by OhioHealth.
NCT02219087 is a NA study that has completed, run by OhioHealth. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02219087, a NA study, has completed, sponsored by OhioHealth.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether liposomal bupivacaine is effective in the management of pain following total knee arthroplasty, as compared to standard of care analgesia.
Primary Outcome
Number of physical therapy (PT) sessions necessary for discharge. A significant decrease in the number of sessions will be defined as ≥ 2. Typically, there are 2 sessions per day, with each patient completing an average of 4-5 sessions during their admission.
Interventions
- DRUG Standard of Care
- DRUG Liposomal bupivacaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2014-08 |
| Est. Completion | 2016-03 |
| Phase | NA |
What the finished NCT02219087 record still lists
NCT02219087 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Standard of Care is the first listed.
NCT02219087 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02219087 about?
NCT02219087 is a clinical study titled "Liposomal Bupivacaine Versus Standard of Care in Total Knee Surgery". The purpose of this study is to determine whether liposomal bupivacaine is effective in the management of pain following total knee arthroplasty, as compared to standard of care analgesia.
What is the current status of trial NCT02219087?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2014-08. Estimated completion is 2016-03.
What interventions are being tested in trial NCT02219087?
The interventions under investigation include: Standard of Care (DRUG), Liposomal bupivacaine (DRUG).
Who is sponsoring clinical trial NCT02219087?
This trial is sponsored by OhioHealth, which has 20 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02219087's enrollment target sits among peer trials
60 1164th of 2000 higher than 745 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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