Skip to content

Study on the synergistic effect of Biological field effect in clearing damp pain by pain treatment of low back and knee pain

Project of capacity building for sustainable utilization of precious traditional Chinese medicine resources

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033700
Enrollment
Unknown
Registered
2020-06-09
Start date
2020-06-30
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

myofascial pain syndrome

Interventions

Sponsors

China Academy of Chinese Medical Sciences Xiyuan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Diagnostic criteria for myofascial pain syndrome: Main criteria: (1) Chief complaint or multiple area pain; (2) Complaints of pain or pain at the trigger point, paresthesia in the expected distribution area; (3) The palpation of the affected muscles was taut and banded; (4) A point along the tension strip presents a sharp point-like tenderness; (5) At the time of measurement, there was some degree of movement limitation. Secondary criteria: (1) Clinical pain or paresthesias with recurrent complaints of tenderness points; (2) Local spasm response was induced by transverse grasp or acupuncture into the trigger point of the strip; (3) Stretch the muscle or inject the trigger point to ease the pain. (4) Myofascial pain syndrome can be diagnosed by meeting the above 5 primary and at least 1 secondary criteria. 2. Patients with myofascial pain syndrome should meet the above diagnostic criteria and be tested voluntarily. 3. Aged 18-75 years; 4. Comply with the requirements of medical ethics.

Exclusion criteria

Exclusion criteria: 1. Patients with hypertension, severe cardiovascular and cerebrovascular diseases, superficial skin open wounds, infectious diseases and bleeding tendency; 2. Suspected or confirmed vertebral or spinal canal tumors, tuberculosis and severe osteoporosis; 3. Pregnant or lactating women with allergic constitution; 4. Those who are suffering from neurological or psychiatric diseases and cannot cooperate with the doctor's guidance or treatment; 5. Those who have difficulty understanding the contents of the scale and are unable to judge their own pain degree; 6. Women who are menstruating during the 2-week treatment cycle and may affect the assessment of pain.

Design outcomes

Primary

MeasureTime frame
McGill pain questionnaire;

Secondary

MeasureTime frame
Quality of life;Adverse events;

Countries

China

Contacts

Public ContactXiao Jing

China Academy of Chinese Medical Sciences Xiyuan Hospital

58280244@SINA.COM+86 010-62835149

Outcome results

None listed

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