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Postoperative Pain Control With Lipossomic Extended Release Bupivacaine Summary Randomized trial of intraoperative intercostal block with bupivacaine with epinephrine compared to lipossomal extended release bupivacaine.
View Full Description Full Description Patients undergoing minimally invasive thoracic surgery will be randomized to receive 0.05% bupivacaine with 1:200,000 epinephrine (control group) or extended release lipossomal bupivacaine. Primary outcomes are postoperative pain measured by visual analog scale, amount of morphine equivalent narcotics used, and postoperative complications. Patients are excluded if they undergo open thoracotomy, or minimally invasive decortication.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Patients who will be undergoing minimally invasive thoracic surgery Patients who will be undergoing minimally invasive thoracic surgery Exclusion Criteria: Open surgery Chronic use of narcotics Use of pregabalin or similar Significant liver or kidney dysfunction
Check Your Eligibility
Let’s see if you might be eligible for this study.
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There is 1 Location for this study
Methodist University Hospital Memphis Tennessee, 38104, United States
More Info How clear is this clinincal trial information?
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