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Clinical study of ultrasound-guided cervical nerve root block combined with blade needle release in the treatment of radicular pain of cervical spondylotic radiculopathy

Clinical study of ultrasound-guided cervical nerve root block combined with blade needle release in the treatment of radicular pain of cervical spondylotic radiculopathy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037281
Enrollment
Unknown
Registered
2020-08-27
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-10-13

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

Conditions

Cervical spondylotic radiculopathy

Interventions

Group 1:Ultrasound guided cervical nerve root block
Group 2:Ultrasound guided cervical nerve root block and blade needle release were used

Sponsors

East Hospital of Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: According to the relevant standards of nerve root type cervical spondylosis in "diagnostic efficacy standard of traditional Chinese medicine" (2017 Edition) and "guiding principle of clinical research on treatment of cervical spondylosis with new Chinese medicine" (2002 Edition) formulated by the State Administration of traditional Chinese medicine: (1) There are obvious symptoms of cervical spondylotic radiculopathy, pain and numbness of neck, shoulder and arm, radiation to the upper limbs, decreased sensation and muscle strength of the affected area, and neck movement; (2) intervertebral foraminal compression pain was found in the traction test; (3) They are 30-75 years old, male and female.

Exclusion criteria

Exclusion criteria: (1) Patients with serious basic diseases that affect the judgment of peripheral nerve injury, such as cerebral infarction, diabetes mellitus, peripheral neuropathy, etc.; (2) patients who received other treatments during the trial or did not meet the requirements, which affected the observation indexes; (3) patients with severe heart, liver, kidney, blood system diseases, mental diseases, and coagulation dysfunction; (4) Patients with shoulder hand syndrome with atypical neck and shoulder pain.

Design outcomes

Primary

MeasureTime frame
Sensory nerve quantitative detector;

Secondary

MeasureTime frame
Tanaka Jingjiu 20 score method;Digital assessment scale;Cervical spine dysfunction index;Clinical assessment scale for cervical spondylosis;

Countries

China

Contacts

Public ContactZhu Yi

East Hospital of Shanghai Sixth People's Hospital

doctorzhuyi@163.com+86 18930174190

Outcome results

None listed

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