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Randomized controlled study of acupuncture combined with medicine for cervical spondylotic radiculopathy based on qi and blood theory

Randomized controlled study of acupuncture combined with medicine for cervical spondylotic radiculopathy based on qi and blood theory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084021
Enrollment
Unknown
Registered
2024-05-09
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

cervical spondylotic radiculopathy

Interventions

Acupuncture combined with traditional Chinese medicine group:1. Acupuncture scheme Acupuncture point selection refers to Acupuncture Therapeutics and our team's clinical experience for many years. We
The operator disinfected his hands, washed his fingers with soapy water, and then wiped his fingers with 75% ethanol cotton balls. Sterilize the acupuncture site, and use 75% ethanol cotton balls to c
Use 0.30 mm×50 mm disposable sterile acupuncture and moxibustion to directly prick the acupuncture points for 1-2 inches, after lifting, inserting and twisting, leave the needle for 30 minutes
Out of the needle, the order is first up and then down, first inside and then outside, holding the sterilized cotton ball in your left hand and pressing the acupoint. Hold the needle handle with your

Sponsors

Beijing Tsinghua Changgeng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with cervical spondylotic radiculopathy who meet the above diagnostic criteria of western medicine and TCM syndrome differentiation criteria; 2. Patients aged 25 to 70 years old, male or female; 3. Conscious and able to understand the content of the scale; 4. The patient informed consent to participate in this clinical study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who are known to have allergic history to drugs with similar components and chemical structures; 2. Patients with hepatic and renal insufficiency, including those with slightly elevated levels of ALT, ALP, eGRr and SCR; 3. Hematopoietic diseases; 4. Severe metabolic diseases and endocrine diseases; 5. Patients with severe heart and brain diseases; 6. Patients with low immunity; 7. Staff directly involved in this study; 8. Pregnant or women of childbearing age with positive pregnancy test and lactating women; 9. Currently participating in other clinical studies or participating in other clinical researchers within 3 months; 10. Other circumstances judged by the researcher as unsuitable for participating in clinical research.

Design outcomes

Primary

MeasureTime frame
Northwick Park Neck Pain Questionnaire after 0 weeks of enrollment and 4 weeks of treatment;

Secondary

MeasureTime frame
Northwick Park Neck Pain Questionnaire after 3 and 6 months of treatment;Evaluation of MOS SF-36 quality of life score at 4 weeks, 3 months and 6 months.;Clinical Assessment Scale for Cervical Spondylosis after 4 weeks, 3 months and 6 months of treatment;Syndrome score of traditional Chinese medicine;

Countries

China

Contacts

Public ContactLiu Cheng

Beijing Tsinghua Changgung Hospital

lca01217@btch.edu.cn+86 136 8145 4687

Outcome results

None listed

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