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NCT03587584 · ClinicalTrials.gov registry record · Phase 4
Liposomal Bupivacaine Interscalene Blocks for Rotator Cuff Repair
A Phase 4 study, sponsored by University of Minnesota.
- Completed
- Registry status
- Phase 4
- Development phase
- 80
- Enrollment target
NCT03587584 is a Phase 4 study that has completed, run by University of Minnesota. The registered enrollment target is 80 participants.
The verdict
NCT03587584, a Phase 4 study, has completed, sponsored by University of Minnesota.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 80 participants
- Enrollment target
Study Summary
The purpose of this study is to compare pain control after arthroscopic rotator cuff repair surgery using either liposomal bupivacaine or bupivacaine when injected in an interscalene block. Both medications, liposomal bupivacaine and bupivacaine, are standard of care in these types of surgeries.
Interventions
- DRUG Bupivacaine
- DRUG liposomal bupivacaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2018-07-25 |
| Est. Completion | 2021-06-08 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03587584
The ClinicalTrials.gov registry entry for NCT03587584 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Bupivacaine is the first listed.
NCT03587584 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03587584 about?
NCT03587584 is a clinical study titled "Liposomal Bupivacaine Interscalene Blocks for Rotator Cuff Repair". The purpose of this study is to compare pain control after arthroscopic rotator cuff repair surgery using either liposomal bupivacaine or bupivacaine when injected in an interscalene block. Both medications, liposomal bupivacaine and bupivacaine, are standard of care in these types of surgeries.
What is the current status of trial NCT03587584?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 80 participants. The study started on 2018-07-25. Estimated completion is 2021-06-08.
What interventions are being tested in trial NCT03587584?
The interventions under investigation include: Bupivacaine (DRUG), liposomal bupivacaine (DRUG).
Who is sponsoring clinical trial NCT03587584?
This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.
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