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Comparison of clinical efficacy of ultrasound guided cervical posterior branch block combined with dry acupuncture for cervical spondylosis

Comparison of clinical efficacy of ultrasound guided cervical posterior branch block combined with dry acupuncture for cervical spondylosis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075934
Enrollment
Unknown
Registered
2023-09-20
Start date
2023-09-20
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

Cervical spondylosis of neck type

Interventions

experimental group:The patient underwent trigger point acupuncture combined with ultrasound-guided cervical nerve posterior branch block treatment. Treat once a week, with a continuous treatment cycle
control group:The patient underwent block treatment of the posterior branch of the cervical nerve. Treat once a week, with a continuous treatment cycle of 2 weeks.

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: ? Meets the diagnostic criteria for cervical spondylosis organized by experts in the editorial department of the Chinese Journal of Surgery; ? The course of the disease is = 3 months; ? NRS score>3 points; ? The efficacy of oral medication alone is not satisfactory; ? Age 18-70 years old, with a body mass index (BMI) between 18.5 and 28kg/m2; ? Agree to participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: ? Excluding patients with other neck diseases such as cervical tumors, osteomyelitis, and other diseases; ? The blood sugar and hypertension of diabetes are not well controlled; ? Individuals with severe skin damage or skin infection at the treatment site; ? Suffering from severe blood system diseases or abnormal coagulation; ? Women during menstruation, pregnancy, or lactation; ? Individuals who experience dizziness or are allergic to the therapeutic drugs used in this study. ? Refuse to participate in this study.

Design outcomes

Primary

MeasureTime frame
Numerical Rating Scale;

Secondary

MeasureTime frame
Northwck Park;Pittsburgh sleep quality index;Neck joint mobility;

Countries

China

Contacts

Public ContactYan Yuan

Affiliated Hospital of Xuzhou Medical University

1046112@qq.com+86 180 5226 8635

Outcome results

None listed

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