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Effect of anaesthetic agents on electrocorticographic epilepsy surgery

Effect of Desflurane vs Propofol on electrocorticographic spikes in ECoG guided intractable Epilepsy Surgery- Prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013141
Enrollment
32
Registered
2018-04-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- diagnosed cases of intractable epilepsy scheduled for epilepsy surgery belonging to age 7-65 years and ASA 1/2 with good neuropsychological assessment (IQ more than 70), without known allergies

Interventions

Intervention1: Desflurane group: In Desflurane group, depth of anaesthesia will be maintained with MAC values of 0.8-1.0 with N2O and opioids. During EcoG recording, N2O will be shut 10 minutes prior

Sponsors

Seth GS Medical College and KEM Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Diagnosed case of medically intractable epilepsy - Well-defined lesions on MRI (hippocampal sclerosis, either focal cortical dysplasia, tumor or gliosis) with defined concordance on inter ictal electroencephalography (EEG), Video EEG. - Single Neurosurgeon discretion of ECoG guided Epilepsy Surgery - ASA 1/2 - Good Neuropsychological assessment (Intelligent Quotient (IQ) score > 70)

Exclusion criteria

Exclusion criteria: - Patients with doubtful concordance or with a more diffuse surgical substrate - Patients with morbid obesity, pregnancy - ASA 3 and above - Known allergy to the anesthetic drugs used.

Design outcomes

Primary

MeasureTime frame
To compare the effect of Desflurane and propofol on Electrocorticographic spikes in patients undergoing epilepsy surgeryTimepoint: ECoG spike onset time Total duration of ECoG recording

Secondary

MeasureTime frame
To evaluate the incidence of awareness during surgeryTimepoint: 24 hours postoperatively

Countries

India

Contacts

Public ContactPallavi Gaur

Seth G S Medical College and KEM Hospital

anitanshetty@yahoo.co.uk9223434852

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026