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Clinical efficacy and mechanism of Acupotomy combined with ointment rub and moxibustion in the treatment of Thoracodorsal Myofascial Pain Syndrome

Clinical efficacy and mechanism of Acupotomy combined with ointment rub and moxibustion in the treatment of Thoracodorsal Myofascial Pain Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082059
Enrollment
Unknown
Registered
2024-03-20
Start date
2022-07-11
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Thoracodorsal Myofascial Pain Syndrome

Interventions

Treatment group:Acupotomy combined with ointment rub and moxibustion
Control group:Acupuncture combined with ointment rub and moxibustion

Sponsors

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 63 Years

Inclusion criteria

Inclusion criteria: (1) Refer to the diagnostic criteria for thoracic dorsal fasciitis issued by the State Administration of Traditional Chinese Medicine in 2012 and the diagnostic criteria of the Chinese Medical Association's Clinical Diagnosis and Treatment Guidelines for Orthopaedics (edited by Qiu Xing, People's Health Publishing House, first edition); (2) Have not been treated with medication in the last 2 weeks; (3) Voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those who did not meet the inclusion criteria; (2) Those who had infections in the local skin where the procedure was applied; (3) Those who had poor glycemic control; (4) Those who had a combination of cardiovascular, cerebrovascular, hepatic, renal, and hematopoietic systems and other serious primary diseases and those who were mentally ill; (5) Those who had a tendency to hemorrhage; (6) Those who were poorly adherent and could not actively cooperate with the examination and treatment.

Design outcomes

Primary

MeasureTime frame
McGill Pain Questionnaire Short-Form;

Secondary

MeasureTime frame
Oswestry disability index (ODI);Cyclooxygenase 2, TNF-a (Tumor Necrosis Factor-a) and IL-1ß (Interleukin-1ß) ;

Countries

China

Contacts

Public ContactJunchen Zhu

The Second Affiliated Hospital of Anhui University of Chinese Medicine

2006zhujc@163.com+86 139 6506 7700

Outcome results

None listed

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