The effect of Liposomal Bupivacaine on the quality of recovery in patients undergoing shoulder arthroscopy

The effect of Liposomal Bupivacaine on the quality of recovery in patients undergoing shoulder arthroscopy
Enrolling By Invitation
18 years - 99 years
All
Phase 3
200 participants needed

Brief description of study

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.

Detailed description of study

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.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: shoulder
  • Age: 18 years - 99 years
  • Gender: All


Updated on 19 Feb 2024. Study ID: 832346
If you need help finding a study or have any questions, please contact us at psom-ocr@pobox.upenn.edu

 

Interested in the study?

Message For Enrolling By Invitation Trial

study is selecting its participants from a population, or group of people, decided on by the researchers in advance.

Contact a study center.