Based on EEG and fMRI technology to investigate the transdermal acupoint stimulation mechanism research

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2200006101

Enrollment

Unknown

Registered

2022-06-12

Start date

2022-06-01

Completion date

Unknown

Last updated

2023-02-20

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

Conditions

healthy subjects

Interventions

Acupuncture group:Acupuncture point stimulation

TEAS group:Transcutaneous electrical acupoint stimulation

Eligibility

Sex/Gender

All

Age

18 Years to 28 Years

Inclusion criteria

Inclusion criteria: ? The ages of 18 and 28 healthy men and not pregnant not lactating women; ? Signed informed consent will be voluntarily.

Exclusion criteria

Exclusion criteria: ? Epilepsy, mental illness claustrophobia or other reasons can't cooperate with researchers; ? People with a cardiac pacemaker, nerve stimulator, artificial metal with metal foreign body inside the body such as heart valve; ? People with hemorrhagic disease or bleeding tendency; ? People has a history of treatment; ? Acupoint stimulation sites on the surface of the skin local infection, chronic inflammation or cannot attach electrodes; ? Do not have informed consent will be.

Design outcomes

Primary

Measure	Time frame
fMRI data;EEG data;	—

Countries

China

Contacts

Public ContactZhang Ming

zm1455@163.com18952170642

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026