Status:
COMPLETED
Impact of Intra- and Postoperative Continuous Infusion of Lidocaine on Analgesia in Vascular Anaesthesia
Lead Sponsor:
Łukasz Krzych
Conditions:
Abdominal Aorta Aneurysm
Abdominal Aorta Atheroma
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The aim of the study is to test the effectiveness and safety of the use of lidocaine infusion in multimodal analgesic management. A group of patients undergoing vascular surgery performed with the cla...
Detailed Description
All enrolled participants will be randomized, using random-number generator, to two groups - group A (intervention - perioperative continuous infusion of lidocaine) and group B (without intervention -...
Eligibility Criteria
Inclusion
- Written informed consent
- Vascular surgery on aorta or iliac artery
- Proximal anasthomosis of a by-pass in the abdominal cavity
Exclusion
- Contraindications for administration of lidocaine (according to Summary Product Characteristics)
- Preoperative administration of any pain relief medication in patient, especially opioides (excluding pre-analgesia)
- Heart block second or third-degree, previous pacemaker implantation, chronic atrial fibrillation
- Antiarrhythmic medication on regular basis (excluding b-blockers prescribed due to coronary artery disease)
- Other health problems: chronic heart failure (ejection fraction LVEF\<30%), epilepsy or any episode of seizure, chronic renal failure (AKIN 3-5), chronic liver failure ( class B or C in the Child-Pugh classification), Myasthenia gravis, hypoproteinemia,
- Cognitive or mental dysfunction, that prevents proper cooperation.
Key Trial Info
Start Date :
January 29 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 2 2022
Estimated Enrollment :
87 Patients enrolled
Trial Details
Trial ID
NCT04691726
Start Date
January 29 2019
End Date
July 2 2022
Last Update
December 21 2022
Active Locations (1)
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1
Leszek Giec Upper-Silesia Medical Center of the Medical University of Silesia in Katowice
Katowice, Poland, 40-635