Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument
Cervical Spondylosis
About this trial
This is an interventional treatment trial for Cervical Spondylosis focused on measuring digital acupuncture manipulation therapeutic instrument, cervical spondylosis
Eligibility Criteria
Inclusion Criteria:
- Neck pain with the diagnosis of cervical spondylotic radiculopathy;
- Aged between 18-70 years;
- Have not participated in any drug clinical trials within the last month;
- Voluntarily joining this study with informed consents
Exclusion Criteria:
- A history of cervical spine trauma or have received cervical spine surgery;
- Accompanied by obvious dizziness and spinal cord compression symptoms or imaging findings of spinal cord compression;
- Cervical spondylosis in urgent need of surgery;
- Pregnant women and lactating women;
- A serious heart condition, hepatic disease, renal system disease, hematopoietic system disease, or whole-body malnutrition
- Anticoagulant treatments such as warfarin or heparin use of pacemakers or receiving acupuncture in the past 2 weeks
Sites / Locations
- LongHua Hospital Shanghai University of Traditional Chinese MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Sham Comparator
Digital Acupuncture Instrument Group
Manual Acupuncture Group
Sham Acupuncture Group
The needles will be stimulated manually to achieve de qi (a compositional sensation including soreness, numbness, distention and heaviness) and then paired electrodes from the digital acupuncture instrument will be attached to the needle handles and another two adjunct acupoints by the research assistant. The electric current will be increased until the needles begin to vibrate slightly.
Patients in the MA group will undergo similar procedures as the EA group except that no current will be output from the instrument.
Patients in the SA group will receive non-invasive acupuncture to avoid de qi.