Liposome Bupivacaine for ANKLE Blocks

Clinical Trial Summary

Postoperative analgesia for hallux valgus surgery (bunionectomy) is inconsistent and may even result in rebound pain when the (ankle) blocks wear off. It is hypothesized that the mixture of bupivacaine and liposome bupivacaine increases the extent and duration of postoperative analgesia and decreases opioid consumption as compared to bupivacaine alone or to general anesthesia.

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Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
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NCT number	NCT03106545
Study type	Interventional
Source	New York School of Regional Anesthesia
Contact
Status	Completed
Phase	Phase 2
Start date	January 2, 2017
Completion date	October 31, 2017

Liposome Bupivacaine for ANKLE Blocks

Clinical Trial Summary

Clinical Trial Description

Study Design

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