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Clinical Study on the Treatment of Cervical Spondylopathy by Wearable Wrist-ankle Electronic Acupuncture and Analgesic Therapeutic Apparatus

Clinical Study on the Treatment of Cervical Spondylopathy by Wearable Wrist-ankle Electronic Acupuncture and Analgesic Therapeutic Apparatus

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005604
Enrollment
Unknown
Registered
2022-02-04
Start date
2022-02-04
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

cervical spondylosis

Interventions

test group:Wearable wrist-ankle electronic acupuncture analgesia treatment device + manual therapy
control group:Conventional wrist-ankle acupuncture + manual therapy

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age = 20 years old and = 70 years old, regardless of gender; 2. Those who meet the diagnostic criteria for cervical spondylosis of cervical type or radiculopathy; have pain symptoms and VAS score = 4 points, and have no indication for surgery. 3. Those who did not take painkillers within 2 weeks before enrollment; 4. Those who voluntarily participate in this project and sign the informed consent form of the clinical trial;

Exclusion criteria

Exclusion criteria: 1.Neck pain caused by other diseases; 2.Patients with other serious diseases, such as tumor, tuberculosis, ankylosing spondylitis, patients with serious cardiovascular and cerebrovascular, liver, kidney and other serious life-threatening primary diseases; 3.Persons with cognitive, mental or communication dysfunction; pregnant and lactating women; 4.Those who have local skin damage or are not suitable for acupuncture massage; 5.Those who have participated in or are participating in other clinical trials 1 month before enrollment;

Design outcomes

Primary

MeasureTime frame
Neck Disability Index, NDI;Visual Analogue Scale/Score,VAS;

Secondary

MeasureTime frame
range of motion of cervical spine;

Countries

China

Contacts

Public ContactZhanghong
zhanghongdoctor@sina.com18930566930

Outcome results

None listed

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