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Clinical evaluation of moxibustion combined with modified Wu-Qin-Xi in the treatment of cervical spondylopathy based on the theory of bones and muscles

Clinical evaluation of moxibustion combined with modified Wu-Qin-Xi in the treatment of cervical spondylopathy based on the theory of bones and muscles

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034258
Enrollment
Unknown
Registered
2020-06-29
Start date
2019-07-15
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

cervical spondylosis

Interventions

Sponsors

Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic and treatment standards of integrated Traditional Chinese and Western medicine for cervical spondylosis; (2) The chief complaint was neck pain and discomfort; (3) Males and females aged between 18 and 45 years are acceptable; (4) Visual analog neck pain score (VAS) >=3; (5) The course of disease is 3 months or more; (6) Willing to actively cooperate with the research and agree to sign the informed consent. Note: All the patients included in this study must meet the above 6 criteria.

Exclusion criteria

Exclusion criteria: (1) Patients with bleeding tendency, moxibustion allergy constitution and skin diseases; (2) Patients who received neck treatment for neck pain within 1 month before enrollment; (3) Complicated with serious organic lesions such as malignant tumors and fractures, or serious primary diseases such as hypertension and diabetes; (4) Those who have had family planning for half a year, pregnant women and lactating women; (5) Persons with mental retardation or mental retardation who cannot cooperate to complete the questionnaire and examination; (6) Those who have participated in other clinical trials within 3 months before enrollment. Note: Patients who meet any of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
Visual Analogus Scale;

Secondary

MeasureTime frame
Neck Disabilitv Index;Cervical range of motion;

Countries

China

Contacts

Public ContactYang Shen-Qiao

Chengdu University of Traditional Chinese Medicine

346307377@qq.com+86 13880873479

Outcome results

None listed

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