The goal of this clinical trial is to learn about the pharmacokinetics of levobupivacaine in newborns during the continus caudal epidural analgesia. This type of analgesia is used for severly ill newborns. There is a need to lower the opioid doses for this population who is undergoing the surgery due to the life threading indication. In some cases it is considered to use the epidural analgesia for the sake of the patient. The main question is: Is the commonly used dosing of 0,25% levobupivacaine in dose 0,2-0,3mg/kg/h the ideal dosing for these patients? Is this type of dosing of epidural analgesia safe and effective for newborns?
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
24
The blood draws in specified time points
University hospital Motol
Prague, Czechia
Safety
AE, SAE monitoring, opioid intake monitoring
Time frame: 144 hours
Effectivity
Pain managment monitoring - Comfort Neo Scale
Time frame: 144 hours
Neurotoxicity
Follow up visits with basic neurology examination
Time frame: up to 5 years
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