Efficacy of Electroacupuncture in NMOSD Patients With Pain: Study Protocol
Neuromyelitis Optica Spectrum Disorders, Pain
About this trial
This is an interventional treatment trial for Neuromyelitis Optica Spectrum Disorders
Eligibility Criteria
Inclusion Criteria: people diagnosed as NMOSD according to the International Panel for NMO Diagnosis (IPND) criteria.[21] NRS≥4. people were treated with stable doses of biological therapy and/or prednisone, with no regimen adjustment within 30 days prior to enrollment. people did not adjust any standard pain medication combinations, including antiepileptic drugs, antidepressants, and opioids, within 30 days before enrollment. people or their families provided written informed consent. Exclusion Criteria: people enrolled in other clinical studies. people with low cognitive or mental ability. people who became pregnant during the study period, breastfed, or planned to become pregnant. people with serious diseases related to the heart, liver, kidney or hematopoietic system. people with diabetic peripheral neuropathy.
Sites / Locations
- Guangdong Provincial Hospital of Chinese Medicine
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
the electroacupuncture group
the sham electroacupuncture group
electroacupuncture were inserted into bilateral Zusanli (ST36), Sanyinjiao (SP6), Hegu (LI4) and Quchi (LI11), and Yintang (EX-HN3). Electroacupuncture parameters selected the sparse wave, the frequency was 4 Hz, the stimulation intensity was tolerated by the patient.
According to the previous trial,[19] sham acupoints were 1cm away from the level of the acupoints used in the EA group, which avoided the area corresponding to any of the 14 meridians of TCM. The insertion of the needle was shallower (less than 0.2cm) and had similar pain to that of normal needle insertion. The stimulation intensity was 0mA. However, the model of electroacupuncture, the frequency, and duration of treatment in the SEA group were identical in the TA group.