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Clinical Trials/ITMCTR2200005604
ITMCTR2200005604
Not yet recruiting
Phase 1

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

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicin0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
cervical spondylosis
Sponsor
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicin
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

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

Eligibility 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

  • 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;

Outcomes

Primary Outcomes

Not specified

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