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Myofascial trigger point acupuncture for the treatment of thoracodorsal mofascial pain sndrome: a clinical randomized controlled trial

Clinical efficacy evaluation of acupuncture of myofascial trigger point in the treatment of thoracodorsal mofascial pain sndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001751
Enrollment
Unknown
Registered
2025-09-15
Start date
2025-09-30
Completion date
Unknown
Last updated
2025-10-13

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

Sham acupuncture group:Sham acupuncture
Myofascial trigger point acupuncture group:Myofascial trigger point acupuncture

Sponsors

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

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria; (2) Chest and back pain (with the line from the spinous process of the 7th cervical vertebra to the acromion on both sides as the upper boundary the spinous process of the 12th thoracic vertebra the line from the lower edge of the 12th rib to the anterior edge of the 11th rib as the lower boundary and the area composed of the spine and its posterior and soft tissues on both sides) which may involve pain in other parts as the main complaint; (3) 20= age = 70 years old both male and female; (4) The degree of chest and back pain/discomfort was scored by visual analogue scale (VAS) and the pain level was 3 or above in 5 out of every 7 days; (5) The course of the disease is more than 3 months; (6) In the past 2 weeks no relevant treatment for the disease has been carried out; (7) Good compliance willing to cooperate with the study and the patient signed the informed consent form. Note: Patients who meet the above 7 criteria at the same time can be included in this study.

Exclusion criteria

Exclusion criteria: (1) Those under the age of 20 and over 70 years old as well as pregnant and lactating women and those who have childbearing requirements in the past six months; (2) Combined with serious other organic lesions including malignant tumors tuberculosis fractures osteomyelitis etc.; (3) Serious primary diseases such as cardiovascular and cerebrovascular liver kidney and hematopoietic system; (4) Those with mental and intellectual disabilities who are unable to cooperate with the questionnaire; (5) Patients with hemophilia or coagulation disorders allergies and skin diseases; (6) Chest and back pain caused by other organic diseases. (7) Those who are participating in other clinical trials. Note: Patients who meet any of the above criteria are excluded.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Score;

Secondary

MeasureTime frame
Pressure Pain Threshold;The number and dose of analgesics used during the study period and disease-related treatments administered during follow-up;12-item Short Form Health Survey;oswestry disability index;Pittsburgh sleep quality index;pain anxiety symptoms scale;

Countries

China

Contacts

Public ContactYong Nie

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine

2006zhujc@163.com18056096682

Outcome results

None listed

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