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A Clinical Randomized Controlled Trial Study on Visualized Needle-Knife Therapy for Cervical Spondylosis Based on the Jin-Gu Imbalance Theory

A Clinical Randomized Controlled Trial Study on Visualized Needle-Knife Therapy for Cervical Spondylosis Based on the Jin-Gu Imbalance Theory

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000935
Enrollment
Unknown
Registered
2026-04-12
Start date
2025-10-15
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

cervical spondylosis

Interventions

Visualization Needle Knife Group:Image-guided needle knife therapy
Acupuncture Knife Group:needle knife therapy

Sponsors

Jiangxi University of Traditional Chinese Medicine Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1) Those who meet the diagnostic criteria for cervical spondylosis; 2) 18 years = age = 55 years, both genders are acceptable; 3) Those with a negative Adson test; 4) Pain intensity score during neck movement: 3 = NRS = 6; 5) Those who have not used medications or external treatments for neck discomfort in the past month; 6) Willing to participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Patients with severe underlying diseases (including myocardial infarction, stroke, congestive heart failure, severe chronic obstructive pulmonary disease, liver or kidney failure, and malignant tumors, etc.); 2) Patients with local skin erythema, erosion, infection, muscle necrosis, deep tissue abscess, or open injuries; 3) Patients with intracranial or extracranial organic lesions, such as tumors, tuberculosis, infections, fractures, or dislocations; 4) Patients with positive flexion or rotation tests of the neck; 5) Patients with coagulation disorders or severe hematological diseases; 6) Patients with a history of shoulder or cervical surgery or specific cervical spine conditions; 7) Pregnant or lactating women; 8) Patients with mental disorders who are unable to cooperate; 9) Patients participating in other clinical studies simultaneously; 10) Patients deemed unsuitable for participation in this trial by the investigator for other reasons.

Design outcomes

Primary

MeasureTime frame
numerical rating scale, NRS;Neck Disability Index,NDI;

Secondary

MeasureTime frame
The number of cases where the NRS score decreased by 2 points compared to before treatment.;Short Form-12,SF-12;Pittsburgh Sleep Quality Index ,PSQI;Self-Rating Anxiety Scale,SAS;Efficacy Expectation Scale;

Countries

China

Contacts

Public ContactLiu Fushui

Jiangxi University of Traditional Chinese Medicine Affiliated Hospital

lfstcm@163.com15270889717

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026