Prospective, double-blind, randomized-controlled study for pediatric cases scheduled for brain tumor excision with the aid of electrocorticography (ECOG). Intraoperative ECOG has been used in an effort to localize the site of epileptogenicity through the demonstration of Interictal Epileptiform Discharges (IED) persistence, frequency, and distribution. During ECOG, pharmaco-activation may be required in order to activate Interictal Epileptiform Abnormalities (IEAs). Frequency of IEAs will be measured for each drug. The effects of anesthetic agents on intraoperative ECOG, as we assume that fentanyl will be superior to ketamine.
Brain tumors can be responsible for epilepsy refractory to medical therapy. These are typically slow-growing tumors, and surgery aims to cure the patient's seizure disorder. One of the main uses of electrocorticography is mapping the cortical regions associated with epileptiform activity. This information is used to plan resection boundaries. Electroencephalography (EEG) electrodes are placed directly on the cortical surface, and epileptiform activity is identified, and this can guide the extent of resection. This technique is referred to as intraoperative electrocorticography (IOECOG). IOECOG has been used to localize the site of epileptogenicity through the demonstration of Interictal Epileptiform Discharges (IED) persistence, frequency, and distribution. As the intraoperative time is short, clinical seizures are usually not captured by ECOG, but the presence and location of IEAs can be used to localize the epileptogenic focus and guide the resection. During ECOG, pharma coactivation may be required to activate IEAs. Fentanyl and ketamine can be used for this
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
QUADRUPLE
Enrollment
88
Fentanyl, Intravenous bolus administration at a dose of 1 microgram per kilogram of body weight administered once before spike stimulation and another time after resection of epileptic foci for spike stimulation.
Ketamine, Intravenous bolus administration at a dose of 0.5 milligram per kilogram of body weight administered once before spike stimulation and another time after resection of epileptic foci for spike stimulation.
Children's Cancer Hospital Egypt 57357
Cairo, Egypt
Children Cancer Hospital 57357
Cairo, Egypt
Effect of fentanyl and ketamine on frequency of spike activation during intraoperative ECOG
The frequency of spikes will be recorded at baseline (before using the drug) and after using the drug before resection. After resection of the epileptic foci, restimulation with the drug will be done and spikes will be recorded.
Time frame: 18 months
Effect of fentanyl and ketamine on amplitude of the spikes activated during intraoperative ECOG.
The amplitude of spikes will be recorded at baseline (before using the drug) and after using the drug before resection. After resection of the epileptic foci, restimulation with the drug will be done, and the spike amplitude will be recorded.
Time frame: 18-month
Effect of fentanyl and ketamine on number of leads with activated spikes during intraoperative ECOG.
The number of leads with activated spikes will be recorded at baseline (before using the drug) and after using the drug before resection. After resection of the epileptic foci, restimulation with the drug will be done, and the number of leads with activated spikes will be recorded.
Time frame: 18-months
The effect of fentanyl and ketamine on blood pressure is to be measured with the drug administered for stimulation.
The effect of fentanyl and ketamine on blood pressure will measured pre- and post-drug administration.
Time frame: 18 months
The effect of fentanyl and ketamine on heart rate is to be measured with the drug administered for stimulation.
The effect of fentanyl and ketamine on heart rate will be measured pre- and post-drug administration.
Time frame: 18-month
The effect of fentanyl and ketamine on recovery time.
The effect of fentanyl and ketamine on recovery time will be measured.
Time frame: 18 month
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