Analgesic Efficacy of Erector Spinae Plane (ESP) Block vs Intravenous Lignocaine Infusion in Video- Assisted Thoracoscopy (VATS)
Status: Recruiting
Location: See location...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The goal of this clinical trial is to compare analgesic efficacy of erector spinae plane (ESP) block vs intravenous lignocaine infusion in video- assisted thoracoscopy (VATS. The main goals are to compare post- operative pain scores and cumulative post- operative opioid doses in both groups
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Age \>18
• VATS for tumor resection or partial lung resection in emphysema
• Written, informed consent obtained 1 day prior to surgery
Locations
Other Locations
Poland
National Medical Institute of the Ministry of the Interior and Administration
RECRUITING
Warsaw
Contact Information
Primary
Antoni Okniński, MD
antoniokninski@gmail.com
608310346
Backup
Antoni Okniński, MD
antoniokninski@cskmswia.gov.pl
608310346
Time Frame
Start Date: 2024-04-11
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 60
Treatments
Active_comparator: ESP block group
under general anaesthesia, preoperative ultrasound(USG) guided ESP blockade at Th5, single shot of 30 ml 0,3 % bupivacaine (not exceeding the maximum dose of 2 mg/kg of bupivacaine) with adrenaline 5 µg/ml and dexamethasone 0,15 mg/kg intravenously, post-operative infusion of 0,9% NaCl for 6 hours, infusion rate set as if it were lignocaine 1,5 mg/kg/h
Active_comparator: Lignocaine infusion group
pre-induction lignocaine bolus of 1,5 mg/kg i.v. and dexamethasone 0,15 mg/kg intravenously, intraoperative infusion of lignocaine 2 mg/kg i.v., post-operative infusion of lignocaine 1,5 mg/kg i.v. for 6 hours
Related Therapeutic Areas
Sponsors
Leads: Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland