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Clinical Trials/ITMCTR2200006101
ITMCTR2200006101
Not yet recruiting
Phase 1

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

Xuzhou Rehabilitation Hospital0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
healthy subjects
Sponsor
Xuzhou Rehabilitation Hospital
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
Xuzhou Rehabilitation Hospital

Eligibility 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

  • ? 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.

Outcomes

Primary Outcomes

Not specified

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