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High Selective Subiculum SEEG Guided RF-TC for mTLE-HS

The Efficacy and Safety of Subiculum Stereotactic-EEG Guided Radio-frequency Thermocoagulation for Mesial Temporal Lobe Epilepsy With Hippocampus Sclerosis: A Prospective, Single-Arm Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06558864
Enrollment
20
Registered
2024-08-19
Start date
2024-08-09
Completion date
2027-08-20
Last updated
2024-08-19

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

Conditions

Epilepsy, Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis

Keywords

Radio-frequency thermocoagulation, Stereoelectroencephalography, Subiculum

Brief summary

The primary objective of this research is to study the efficacy and safety of Stereotactic EEG (SEEG) guided radio-frequency thermocoagulation (RF-TC) of Subiculum as adjunctive therapy for reducing the frequency of seizures in drug-resistant temporal lobe epilepsy with Mesial temporal lobe epilepsy with hippocampal sclerosis (mTLE-HS).

Detailed description

Mesial temporal lobe epilepsy (mTLE) is the most classical subtype of temporal lobe epilepsy, which is the indication of surgical intervention after evaluation. This project aims to include 20 participants, and evaluate the effectiveness and safety of Stereotactic EEG (SEEG) guided radio-frequency thermocoagulation (RF-TC) of Subiculum in patients with mesial temporal lobe epilepsy with hippocampal sclerosis through A prospective, interventional, unblinded, single-arm clinical trial. It is expected to provide new therapeutic options for patients with mTLE-HS with alternative treatment options.

Interventions

PROCEDURESubiculum RF-TC

SEEG implantation after evaluation, record the interictal and ictal EEG, and perform Subiculum RF-TC.

Sponsors

Xuanwu Hospital, Beijing
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Participants are between the ages of 14 -65 years of age * Refractory to anti-seizure medications (ASMs). * Persistence of disabling seizures at least 2 times per month during the Baseline Phase,with no more than 30 days between seizures during the Baseline Phase. * Hippocampal atrophy on MRI T1 imaging with increased ipsilateral mesial signal on T2 imaging * Interictal EEG shows focal or lateralized spikes on temporal, frontal zone, or sphenoid electrode * Ictal EEG onset is focal or lateralized on the ipsilateral side * Ipsilateral temporal focal hypometabolism on PET * Must be agreed by a consensus of ipsilateral mesial temporal origin by a multidisciplinary discussion

Exclusion criteria

* Diagnosed with generalized or hereditary epilepsy with ion channel gene mutations; * Psychogenic non-epileptic seizures within 12 months; * Presence of implanted electrical stimulation medical device anywhere in the body (e.g., pacemaker, spinal cord stimulator, responsive neurostimulation) or any metallic implants in the head (e.g., aneurysm clips, cochlear implants). Note: Vagal nerve stimulators are allowed if the parameter remains stable for at least 3 months prior to the screening visit; * Risk factors that would put the participant at risk for intraoperative or postoperative bleeding. (e.g., coagulation abnormalities, etc.) or the need for chronic anticoagulation or antiplatelet aggregation medications; * IQ \< 55 or severe cognitive dysfunction, unable to complete the study; * Diagnosed with a progressive neurological disorder (including progressive Rasmussen's encephalitis, etc.); * Diagnosed with a severe neuropsychiatric disorder such as dementia, major depression (admission to a psychiatric specialty/hospital within 5 years or any suicidal or self-injurious tendencies), schizophrenia, or neurodegenerative disorders; * Diagnosed with other serious physical disorders, internal diseases or severe abnormalities in liver or kidney function; * Pregnant, or planning to pregnant within 2 years; * Participation in another clinical study within 3 months; * Not suitable for enrollment as assessed by the multidisciplinary team of the center.

Design outcomes

Primary

MeasureTime frameDescription
Seizure frequency (SF28)Up to 1 year after subculum-SEEG Guided RF-TCSeizure frequency (SF28) is defined as seizure count per month (28-day) period. The SF28 is calculated as follows, where D=total number of days for which seizure information is collected for the specific 28-day interval: SF28=(Total number of seizures in D days/D)\*28. In addition, the baseline seizure frequency is defined as mean of 3-month SF28 in the baseline period. The seizure frequency in double-blind phase is defined as SF28 per month during the double-blind period. Percent change in seizure frequency=100\*(double-blind SF28-baseline SF28)/baseline SF28.

Secondary

MeasureTime frameDescription
Life quality evaluationUp to 1 year after subculum-SEEG Guided RF-TCPercentage change from baseline in Quality of Life in Epilepsy-31 inventory (QOLIE-31) score.
Cognitive function evaluation (MMSE)Up to 1 year after subculum-SEEG Guided RF-TCPercentage change from baseline in Mini-Mental State Examination (MMSE) score.
Seizure Responder RateUp to 1 year after subculum-SEEG Guided RF-TCThe proportion of patients with a ≥ 50% reduction from Baseline in seizure frequency.
Adverse EventsUp to 1 year after subculum-SEEG Guided RF-TCRate of adverse events which were judged to be study-related throughout the study.
Incidence of Sudden Unexpected Death in Epilepsy (SUDEP)Up to 1 year after subculum-SEEG Guided RF-TCThe number presented is for Definite and Probable SUDEP. The rate is calculated per 1000 subject years of follow-up.
Cognitive function evaluation (MoCA)Up to 1 year after subculum-SEEG Guided RF-TCPercentage change from baseline in Montreal Cognitive Assessment (MoCA) score.

Contacts

Primary ContactLiankun Ren
renlk2022@outlook.com+86 13681576621

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026