Skip to content

Atlas of Intracranial Recordings on Cortical Responses After Functional tACS

An Atlas of Cerebral Responses to the Stimuli of the tACS Recorded by SEEG

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04560959
Acronym
AIRCRAFT
Enrollment
30
Registered
2020-09-23
Start date
2020-09-20
Completion date
2021-12-01
Last updated
2020-09-23

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

Conditions

Transcranial Alternating Current Stimulation

Brief summary

By analyzing the SEEG recordings, we explore the range of cortical functional responses to strings of 77.5Hz stimulations delivered by tACS,

Interventions

DEVICEtACS

tACS would be performed to epilepsy patients who have already received implantation of the SEEG electrodes

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 60 Years
Healthy volunteers
No

Inclusion criteria

* All epileptic patients that would receive the implantation of SEEG electrodes, regardless of the seizure locations; * There was no metal implantation before; * Eligible for MRI examination; * No other lesional neurological disorders; * Could be well informed by the study protocols.

Exclusion criteria

* Suffered from any other mental illnesses prior to the enrollment; * Those suffering from the serious or unstable organic diseases; * Pregnant or lactation women, and those who have a plan of pregnant; * Patients with central nervous system tumors, acute brain injury or infection; * Skin injured, or allergic to the exposure of the conductive gel; * Those with implanted devices; * Those who received modified electrical convulsive therapy, or TMS within the recent one month; * The score of item 3 (suicidal item) in HAMD-17 equal or greater than 3; * Enrolled in any other on going trials; * Other situations evaluated by the researchers as inappropriate to the enrollment

Design outcomes

Primary

MeasureTime frameDescription
Changes of intracranial activitiesWithin 250 ms immediately after the stimulation.The change of the power in a band of 0-200 HZ according to the intracranial EEG recording.

Secondary

MeasureTime frameDescription
Frequency of the epileptic discharges50 minutes during the stimulation and 50 minutes of the interictal baseline before the intervention during the same hour of the dayTo count the numbers of epileptic discharges within the same duration before and when tACS intervention.
Event related potential (ERP)Baseline: 24 hours before the tACS intervention; Observation: Immediately after the end of the tACS intervention.ERP related to cognitive tasks before and immediately after the tACS intervention

Contacts

Primary ContactP.H. Wei
weipenghu@xwhosp.org+86-010-83198252

Outcome results

None listed

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