Lung Cancer Clinical Trial

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.

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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.

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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

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

50

Study ID:

NCT03560362

Recruitment Status:

Unknown status

Sponsor:

University of Tennessee Health Science Center

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There is 1 Location for this study

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Methodist University Hospital
Memphis Tennessee, 38104, United States More Info
Benny Weksler
Contact
901-448-2918
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

50

Study ID:

NCT03560362

Recruitment Status:

Unknown status

Sponsor:


University of Tennessee Health Science Center

How clear is this clinincal trial information?

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