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To observe the clinical effect of massage therapy on vertebral artery type cervical spondylosis based on sympathetic nerve and vascular adjustment axis

To explore the mechanism of massage therapy for vertebral artery type cervical spondylosis based on the sympathetic nerve-vascular-cell apoptosis regulating axis

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400079373
Enrollment
Unknown
Registered
2024-01-02
Start date
2024-01-02
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Cervical Spondylosis

Interventions

Treatment group:Massage + Functional exercise

Sponsors

The Second Affiliated Hospital of Anhui University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria: the diagnostic criteria of vertebral artery type Cervical spondylosis in the Summary of the Third National Symposium on Cervical Spondylosis, and the criteria of vertebral artery type cervical spondylosis in the Diagnosis and Efficacy Criteria of TCM Diseases; (2) Aged between 30 and 60 years, duration of disease =24 months; (3) No other systemic diseases; (4) No medication or other treatment for nearly 2 weeks; (5) Sign the informed consent and participate in the experiment regularly according to the research requirements.

Exclusion criteria

Exclusion criteria: (1) Patients with other types of cervical spondylosis; (2) Patients with vertigo caused by diseases of ear, brain and eye origin; (3) Patients with heart, liver, kidney and other primary diseases or mental diseases; (4) pregnant and lactating women; (5) Cases that are not suitable for massage treatment; (6) The condition is critical and it is difficult to independently evaluate the effectiveness and safety of treatment; (7) It is difficult to adhere to the established treatment plan and affect the subject.

Design outcomes

Primary

MeasureTime frame
PI; TMFV; PSV; RI ;The functional status and psychological function of the patients were evaluated before and after treatment;Blood pressure, heart rate, body temperature, gastrointestinal motility, pupil size;

Secondary

MeasureTime frame
Comprehensive clinical efficacy evaluation;

Countries

China

Contacts

Public ContactChao Wang

The Second Affiliated Hospital of Anhui University of Chinese Medicine

wangchao@ahtcm.edu.cn+86 136 3708 4001

Outcome results

None listed

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