Evidence map›Paper›PMID 40499969›Full record

ArticleBMJ open2025

Thalamic neural activity and epileptic network analysis using stereoelectroencephalography: a prospective study protocol.

Tomotaka Ishizaki, Satoshi Maesawa, Shun Yamamoto, Takahiro Suzuki, Miki Hashida, Yoshiki Ito, Takafumi Tanei, Ryuta Saito

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Tomotaka IshizakiDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan ishizaki.tomotaka.d8@f.mail.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0001-5346-6451
Satoshi MaesawaDepartment of Neurosurgery, National Health Organization, Nagoya Medical Center, Nagoya, Aichi, Japan.
Shun YamamotoDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Takahiro SuzukiDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Miki HashidaDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Yoshiki ItoDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Takafumi TaneiDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.
Ryuta SaitoDepartment of Neurosurgery, Nagoya University, Nagoya, Aichi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEpilepsy is a prevalent chronic neurological disorder, with approximately one-third of patients experiencing intractable epilepsy, often necessitating surgical intervention. Deep brain stimulation (DBS) of the thalamus has been introduced as a palliative surgical option for seizure control; however, its precise mechanisms remain largely unclear. The thalamus plays a crucial role in coordinating neural networks, both in normal brain function and the propagation of epileptic activity. This study aims to investigate the involvement of the thalamus in epilepsy networks using stereoelectroencephalography (SEEG) to monitor thalamic activity during epileptic seizures in patients with drug-resistant epilepsy. METHODS AND ANALYSIS: This single-arm, non-randomised, prospective, exploratory study will be conducted at Nagoya University Hospital, involving 10 patients undergoing SEEG for presurgical evaluation of drug-resistant epilepsy. Participants must be 18 years or older, have normal cognitive function and provide informed consent. Between 7 and 14 SEEG electrodes, including 2 in the bilateral thalamus, will be implanted in key thalamic nuclei (anterior, dorsomedial, centromedian and pulvinar) using a robotic system. The primary outcome focuses on electroencephalographic findings from the thalamus, emphasising waveform and frequency changes around seizures. Secondary outcomes include postoperative seizure frequency, changes in cognitive function and neuroimaging results. SEEG data will be recorded continuously for 1-2 weeks to capture both ictal and interictal activity. Data analysis will employ t-tests to compare ictal and interictal periods, with p values <0.05 deemed statistically significant. This study seeks to characterise thalamic spectral and connectivity changes during seizures, identify the thalamic subnuclei involved in seizure propagation and explore their association with seizure outcomes, potentially contributing to future DBS candidate selection. By advancing our understanding of the thalamus in epilepsy networks, this research aims to improve DBS interventions, ultimately enhancing seizure control in patients with intractable epilepsy. ETHICS AND DISSEMINATION: This study was approved by the ethics committee of the Nagoya University Graduate School of Medicine (Approval No. 2024-0044). All participants will provide written informed consent prior to enrolment. The results of this study will be disseminated through publication in a peer-reviewed journal and presentations at academic conferences. TRIAL REGISTRATION NUMBER: jRCT1042240024.

Indexed as

Drug Resistant EpilepsyElectroencephalographyNerve NetThalamusAdolescentAdultDeep Brain StimulationFemaleHumansMaleProspective StudiesSeizuresStereotaxic TechniquesYoung AdultNeurologyNeurophysiologyNeurosurgery

Identifiers

PMID40499969
PMCPMC12161333

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.