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Clinical study on the treatment of cervical spondylopathy with Fu's Subcutaneous Needling combined with reperfusion approach based on sEMG evaluation

Clinical study on the treatment of cervical spondylopathy with Fu's Subcutaneous Needling combined with reperfusion approach based on sEMG evaluation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043529
Enrollment
Unknown
Registered
2021-02-21
Start date
2021-02-21
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

cervical spondylopathy

Interventions

Sponsors

The People's Hospital of Gaoming District of Foshan City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria of cervical spondylosis in the 2010 Guidelines for the Diagnosis, Treatment and Rehabilitation of Cervical Spondylosis; (2) Patients aged 18-65 years old; gender is not limited; (3) No other serious diseases; (4) Signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients who have poor compliance and cannot successfully complete the experiment, or who receive other treatments during the experiment; (2)There are other situations that are not suitable to be included in the study.

Design outcomes

Primary

MeasureTime frame
Average electromyography;Mean power frequency;

Secondary

MeasureTime frame
The McGill Pain Questionnaire;

Countries

China

Contacts

Public ContactJiaen Yang

The People's Hospital of Gaoming District of Foshan City

joshua19882006@qq.com+86 757-88883379

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026