The effect of Liposomal Bupivacaine on the quality of recovery in patients undergoing shoulder arthroscopy
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- STATUS
- Enrolling By Invitation
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- participants needed
- 200
Summary
The research study is being conducted to see if using liposomal bupivacaine for the interscalene block will improve the patient pain control and the whole patient’s experience 48 hours after surgery when compared to using the regular Marcaine in addition to the dexamethasone.
Description
You are being invited to participate in a research study because you will be having shoulder arthroscopy (called shoulder scope) and you will receive a nerve block to numb your shoulder and arm as part of your pain control protocol after surgery.
FAQ
Details
| Condition | shoulder |
|---|---|
| Age | 18years - 99years |
| Clinical Study Identifier | TBD |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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