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

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

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041479
Enrollment
Unknown
Registered
2020-12-27
Start date
2020-12-30
Completion date
Unknown
Last updated
2021-03-15

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

Conditions

myofascitis

Interventions

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion 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

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.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;Short Form 36 Health Survey Questionnaire (SF-36);Oswestry Disability Index (ODI);

Secondary

MeasureTime frame
infrared thermography;

Countries

China

Contacts

Public ContactLijun He

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

Yin7like@163.com+86 18819480189

Outcome results

None listed

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