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

Phase 1

• Conditions: myofascial pain syndrome

• Registration Number: ITMCTR2000003386
• Lead Sponsor: China Academy of Chinese Medical Sciences Xiyuan Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: Not specified

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

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.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
McGill pain questionnaire;

Secondary Outcome Measures

Name	Time	Method
Adverse events;Quality of life;