Skip to main content
Clinical Trials/ITMCTR2000004200
ITMCTR2000004200
Recruiting
Phase 1

To observe the effect of massage combined with milli-fire needle on myofascitis of the back region based on infrared thermography technology

The First Affiliated Hospital of Guangzhou University of Chinese Medicine0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
The First Affiliated Hospital of Guangzhou University of Chinese Medicine
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
All

Investigators

Sponsor
The First Affiliated Hospital of Guangzhou University of Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • 1\) The observation subjects were outpatient patients in the department of massage in The First Affiliated Hospital of Guangzhou University of Chinese Medicine.
  • 2\) It conforms to the diagnostic criteria of myofascitis of the back region in the Diagnostic and Therapeutic Criteria of Diseases and Syndromes of Traditional Chinese Medicine.
  • 3\) Patients aged between 20 and 65 years.
  • 4\) VASv \< points.
  • 5\) The patient was sane, understandable, well compliant, voluntarily accepted this therapy, agreed to participate in this clinical study and signed informed consent surgeons.

Exclusion Criteria

  • 1\) There are localized skin infections at the treatment site.
  • 2\) Suffering from serious heart, lung, liver and kidney diseases.
  • 3\) Diabetes, hemophilia, thrombocytopenic purpura or severe osteoporosis.
  • 4\) Pregnancy or lactation.
  • 5\) Rheumatism, osteoarthrosis, tumor and fracture, etc.
  • 6\) Patients with abnormal coagulation function, skin damage or infection at tendon junction are not suitable for milli\-fire needle.
  • 7\) In the last 2 weeks, take non\-steroidal anti\-inflammatory drugs, muscle relaxants, or acupuncture and massage, etc.
  • 8\) Patients who are currently participating in or have participated in other clinical trials in the month prior to this study.

Outcomes

Primary Outcomes

Not specified

Similar Trials