Fu's Subcutaneous Needling on the Myofascial Trigger Points: Lateral Epicondylitis
Lateral Epicondylitis
About this trial
This is an interventional treatment trial for Lateral Epicondylitis focused on measuring Fu's subcutaneous needling (FSN), Myofascial trigger point
Eligibility Criteria
Inclusion Criteria:
1. Subjects older than 20 years of age who can cooperate with the experimental volunteers.
2. Suffering from epicondylitis of the humerus for more than one month, and subjective pain intensity (VAS) greater than 5 points.
3. There is a local tender point at the upper elbow of the elbow, and the isometric resistance test of the forearm to make a spin will induce pain.
4. Under soft tissue ultrasound, the thickness of the common tendon of the extensor carpi muscles is more than 0.15 mm greater than that of the healthy side.
Exclusion Criteria:
1. There are contraindications to general treatment, such as serious medical problems, recent serious trauma, or pregnant women.
2. There has been a history of drug abuse (including excess alcohol) that affects pain assessors.
3. Have received neck, upper back, or upper and lower limb surgery. 4. People with central or peripheral nerve disease. 5. Cognitive impairment, unable to cooperate with the experimenter. 6. Patients currently receiving other treatments for epicondylitis of the humerus.
Sites / Locations
- China Medical University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
FSN: Fu's subcutaneous needling
TENS: Transcutaneous Electric Nerve Stimulation
In this arm, the subjects will receive the intervention of FSN on Day1, Day2 and Day4, in total 3 treatments and will be arrange to take efficacy two assessment on Day8 and Day15, separately.
In this arm, the subjects will receive the intervention of TENS on Day1, Day2 and Day4, in total 3 treatments and will be arrange to take efficacy two assessment on Day8 and Day15, separately.