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Clinical Trials/ITMCTR2100004216
ITMCTR2100004216
Recruiting
Phase 1

Study on the measurement of moxibustion sensation and the relationship between moxibustion sensation-dose-effiect

Hospital of Chengdu Universicity of T.C.M0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Hospital of Chengdu Universicity of T.C.M
Status
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
Female

Investigators

Sponsor
Hospital of Chengdu Universicity of T.C.M

Eligibility Criteria

Inclusion Criteria

  • 1\.Meet the chronic fatigue syndrome diagnostic criteria;
  • 2\.Meet the diagnostic standard of syndrome differentiation of spleen and kidney yang deficiency type;
  • 3\.The age range is 18\-60 years old, female;
  • 4\.Subjects did not receive any treatment which may influence the consequent within 1 month;
  • 5\.Sign informed consent voluntarily;

Exclusion Criteria

  • 1\. Druing pregnant and lactating period;
  • 2\. Having Diseases that have definite influence on TTM results, such as scoliosis, limb deformity, etc;
  • 3\. Can't express subjective discomfort symptoms or can't understand and communicate normally;
  • 4\. Having obviously damaged and scarred skin;
  • 5\. Being allergic to ginger;
  • 6\. Being receiving other clinical trials at the same time.

Outcomes

Primary Outcomes

Not specified

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