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Clinical Observation on Seven-line Acupoint Catgut Embedding in the Neck for Comprehensive Improvement of Symptoms and Signs in Patients with Radiculopathic Cervical Spondylosis

Clinical Observation on the Comprehensive Improvement of Symptoms and Signs of Patients with Nerve - root - type Cervical Spondylosis by Neck Seven - line Point - embedding Therapy (Randomized Controlled Clinical Research Part)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001350
Enrollment
Unknown
Registered
2025-07-09
Start date
2025-07-10
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Cervical Spondylotic Radiculopathy (CSR)

Interventions

Medication Group:Oral Medication
Sham Catgut Embedding Group:Sham Acupoint Catgut Embedding
Catgut Embedding Group:Acupoint Catgut Embedding

Sponsors

Shunyi Hospital of Beijing Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meet the Western medical diagnostic criteria; (2) Aged between 18 and 75 years; (3) No psychotropic drugs taken within 1 week before treatment; (4) Able to cooperate with treatment and data collection; (5) Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Health Conditions 1) Severe cardiovascular diseases including: angina pectoris myocardial infarction or stroke within the past 6 months heart failure symptomatic peripheral vascular disease. 2) Systolic blood pressure =160 mmHg and/or diastolic blood pressure =100 mmHg regardless of hypertension treatment. If under treatment no change in medication within the last 3 months. 3) Liver dysfunction (AST >80 U/L ALT >80 U/L) or renal dysfunction (creatinine >2.5 mg/dL eGFR 210 ml/week for males >140 ml/week for females). 2) History of drug abuse within 1 year. 3) History of blood donation or transfusion within 1 month. 4) Pregnant or lactating including planning to conceive within the next 4 months. 5) Allergy to absorbable surgical sutures or animal proteins. 6) Keloid constitution. 7) Allergic or damaged skin at the implantation site. 8) Inability to use smartphones or the internet. 9) Severe allergy or adverse reactions to study medications. 10) Psychological/behavioral issues that may hinder protocol compliance as judged by the investigator.

Design outcomes

Primary

MeasureTime frame
Neck Disability Index  NDI;

Secondary

MeasureTime frame
Visual Analogue ScaleVAS;YT 20-Point Scale Scoring;TCM Syndrome Score;Electromyography (EMG);McGill Pain Questionnaire SF-MPQ;

Countries

China

Contacts

Public ContactDeng Yue

Shunyi Hospital of Beijing Traditional Chinese Medicine Hospital

1259274456@qq.com15300151605

Outcome results

None listed

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