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To study the changes of sensitization characteristics of patients with Neck Type Cervical Spondylopathy along the Gallbladder meridian

Changes in Gallbladder meridian acupoint sensitization and electroacupuncture intervention effect in patients with Neck Type Cervical Spondylopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025000166
Enrollment
Unknown
Registered
2025-01-25
Start date
2025-03-05
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Neck Type Cervical Spondylopathy

Interventions

Neck Type Cervical Spondylopathy group:none
Healthy group:none

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medicine University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Inclusion criteria of Neck Type Cervical Spondylopathy (1) Meeting the diagnostic criteria of Neck Type Cervical Spondylopathy. (2)Age 18 to 65 years old gender is not limited (3)Clear awareness good compliance willing to cooperate with the study and accept the experimental arrangement; (4)Physical examination may or may not be accompanied by positive signs of the musculoskeletal system (including limited motor function local tender points etc.); (5)The visual analogue Scale (VAS) score was more than 3 points and less than 7 points (ranging from 0 to 10 points); (6)Informed consent and sign informed consent. 2. Inclusion criteria for healthy subjects (1)Age 18 to 65 years old gender is not limited (2)No cervical vertebrae-related diseases were detected and no disease diagnosis was made within 6 months before entering the study. (3)Clear awareness good compliance willing to cooperate with the study and accept the experimental arrangement; (4)Informed consent and sign informed consent.

Exclusion criteria

Exclusion criteria: (1)It does not meet the diagnostic criteria and inclusion criteria of cervical spondylosis. (2)Under 18 years of age or over 65 years of age; (3)2 weeks before the start of the experiment the relevant treatment of the disease or the use of relevant therapeutic drugs; (4)Patients with other types of cervical spondylosis (cervical radiculopathy vertebral artery type cervical spondylosis cervical myelopathy sympathetic cervical spondylosis) or with other serious organic diseases and patients with neck and shoulder pain caused by non-neck diseases; (5)Patients with cardiovascular and cerebrovascular liver kidney digestive system blood system and other serious life-threatening primary diseases or suffering from hemorrhagic diseases or skin diseases or pregnant or lactating women or have a history of cardiac pacemaker implantation; (6)Previous history of neck surgery or neck fracture; (7)Persons with confusion mental disorder or cognitive impairment; (8)The skin at the test site has scars redness swelling heat and pain that affect the test result.

Design outcomes

Primary

MeasureTime frame
Pressure pain threshold;

Secondary

MeasureTime frame
Visual Analogue Scale (VAS);The 12 items Short Form Health Survey(SF-12);Cervical range of motion scale;The Neck Disability Index(NDI);

Countries

China

Contacts

Public ContactLiChaoran

The Third Affiliated Hospital of Zhejiang Chinese Medicine University

crwd44@163.com15557137527

Outcome results

None listed

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