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Atlas of Intracranial Recordings on Cortical Responses After Functional tACS (AIRCRAFT)

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Capital Medical University

Status and phase

Unknown
Phase 2
Phase 1

Conditions

Transcranial Alternating Current Stimulation

Treatments

Device: tACS

Study type

Interventional

Funder types

Other

Identifiers

NCT04560959
LYS-[2020]-051

Details and patient eligibility

About

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

Enrollment

30 estimated patients

Sex

All

Ages

14 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

tACS arm
Experimental group
Description:
The patient would receive strings of tACS stimulations in 77.5 HZ, each string would last for 1 second, followed by an interval of 5 seconds. A total of 600 strings would be sent out to the patients.
Treatment:
Device: tACS

Trial contacts and locations

0

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Central trial contact

P.H. Wei

Data sourced from clinicaltrials.gov

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