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Stereotactic Laser Ablation for Temporal Lobe Epilepsy

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliKuajiri
Wadhamini
Medtronic Navigation, Inc.

Maneno muhimu

Kikemikali

The study is designed to evaluate the safety and efficacy of the Visualase MRI-guided laser ablation system for mesial temporal epilepsy (MTLE).

Maelezo

The purpose of the study is to evaluate the safety and efficacy of the Visualase MRI-guided laser ablation system for necrotization or coagulation of epileptogenic foci in patients with intractable mesial temporal lobe epilepsy.

The study will include approximately 150 adult patients with drug-resistant MTLE treated at selected epilepsy centers across the United States. After the Visualase procedure, patients will be followed for 12 months and evaluated for freedom from seizures, quality of life, adverse events, and neuropsychological outcomes.

Tarehe

Imethibitishwa Mwisho: 10/31/2019
Iliyowasilishwa Kwanza: 07/14/2016
Uandikishaji uliokadiriwa Uliwasilishwa: 07/20/2016
Iliyotumwa Kwanza: 07/25/2016
Sasisho la Mwisho Liliwasilishwa: 11/19/2019
Sasisho la Mwisho Lilichapishwa: 11/21/2019
Tarehe halisi ya kuanza kwa masomo: 11/30/2016
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 04/30/2022
Tarehe ya Kukamilisha Utafiti: 04/30/2022

Hali au ugonjwa

Temporal Lobe Epilepsy

Uingiliaji / matibabu

Device: Treatment

Awamu

-

Vikundi vya Arm

MkonoUingiliaji / matibabu
Experimental: Treatment
Visualase MRI-guided laser ablation procedure
Device: Treatment
All subjects will undergo MRI-guided laser ablation of the amygdala and hippocampus with the Visualase System.

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaAll
Hupokea Wajitolea wa AfyaNdio
Vigezo

Inclusion Criteria:

- History of drug-resistant mesial temporal lobe epilepsy (MTLE)

- If the subject has a vagus nerve stimulator (VNS), must have failed to achieve sustained seizure freedom with the VNS implanted for at least 6 months

- On stable antiepileptic drugs (AEDs) (and/or stable VNS setting, if applicable) and compliant with medication use

- An average of at least 1 complex partial or secondarily generalized seizure compatible with MTLE per month

- Seizure symptoms and/or auras compatible with MTLE

- Video EEG shows evidence of seizures from one temporal lobe consistent with MTLE

- MRI has evidence consistent with mesial temporal lobe sclerosis

- Willing and able to remain on stable AEDs (and stable VNS setting, if applicable) for 12 months following the Visualase procedure

- Willing and able to comply with protocol requirements

- Able to complete study assessments in English or Spanish language

Exclusion Criteria:

- Unwilling or unable to sign the study informed consent form

- Pregnant or intends to become pregnant during the course of the study

- Currently implanted with a device contraindicating MRI

- Progressive brain lesions and/or tumors not associated with epileptic disease state

- History of previous intracranial surgery for treatment of epileptic seizures

- Persistent extra-temporal or predominant contralateral focal interictal spikes or slowing, or generalized interictal spikes on EEG

- Seizures with contralateral or extra-temporal ictal onset on EEG

- Aura and/or ictal behavior suggest an extra-temporal focus

- MRI evidence of epileptogenic, extra-temporal lesions, dual pathology in the temporal lobe, or contralateral hippocampal MRI increased signal and/or loss of architecture

- If additional testing has been performed, results are discordant with the seizure focus scheduled for ablation

- Non-compliance with AED requirements

- IQ < 70

- Dementia or other progressive neurological disease

- Unstable major psychiatric illness, psychogenic non-epileptic seizures, or medical illness that would contraindicate the Visualase procedure or affect the neuropsychological assessments

- Participation in other research that may potentially interfere with SLATE endpoint(s)

- Allergy to gadolinium

Matokeo

Hatua za Matokeo ya Msingi

1. Incidence of qualifying adverse events [12 months]

2. Seizure freedom, defined as Engel Classification of Postoperative Outcome Class I [12 months]

Hatua za Matokeo ya Sekondari

1. Seizure freedom compared to historical controls [12 months]

2. Seizure freedom, including subjects retreated with Visualase [12 months]

3. Change in Boston Naming Test scores [Baseline and 12 months]

4. Change in Rey Auditory Verbal Learning Test scores [Baseline and 12 months]

5. Change in Short Form-36 (SF-36) Health Survey scores [Baseline and 12 months]

6. Change in Quality of Life in Epilepsy (QOLIE-31) scores [Baseline and 12 months]

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