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Local Anesthetic
Lipossomal extended release bupivacaine for Postoperative Pain
Phase 1 & 2
Waitlist Available
Led By Benny Weksler, MD
Research Sponsored by University of Tennessee Health Science Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 90 days post op
Awards & highlights
Study Summary
Randomized trial of intraoperative intercostal block with bupivacaine with epinephrine compared to lipossomal extended release bupivacaine.
Eligible Conditions
- Postoperative Pain
- Lung Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90 days post op
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90 days post op
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Postoperative pain
Secondary outcome measures
Narcotic used
Postoperative complications
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Lipossomal extended release bupivacaineExperimental Treatment1 Intervention
Patients will receive intraoperative intercostal nerve block with lipossomal extended release bupivacaine
Group II: Bupivacaine with epinephrineActive Control1 Intervention
Patients will receive intraoperative intercostal nerve block with bupivacaine
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Bupivacaine
FDA approved
Find a Location
Who is running the clinical trial?
University of Tennessee Health Science CenterLead Sponsor
48 Previous Clinical Trials
25,054 Total Patients Enrolled
University of TennesseeLead Sponsor
189 Previous Clinical Trials
141,979 Total Patients Enrolled
1 Trials studying Postoperative Pain
69 Patients Enrolled for Postoperative Pain
Benny Weksler, MDPrincipal InvestigatorUniversity of Tennessee
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