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Clinical study on the treatment of cervical radiculopathy with two different mechanisms of electrical stimulation based on "synchronous mode" Clinical study

Clinical study on the treatment of cervical radiculopathy with two different mechanisms of electrical stimulation based on "synchronous mode" Clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079936
Enrollment
Unknown
Registered
2024-01-16
Start date
2024-01-20
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

cervical spondylotic radiculopathy

Interventions

synchronizing group:? Firstly, place electrodes according to the NMES treatment procedure standard and adjust to prescription 1 (neuromuscular electrical stimulation)
?: Then, according to the TENS treatment procedure standard, place electrodes and adjust them to prescription 5 (percutaneous nerve stimulation)
?: Simultaneously activate two therapeutic devices with different therapeutic functions, with NMES adjusted to significantly contract muscles without any painful sensation, and TENS adjusted to slight
Non-synchronous group 1:First, therapy was followed by TENS placebo therapy at an interval of 30min, and then TENS therapy was followed by NMES placebo therapy. The patients were treated once a day fo
Non-synchronous group 1:First, TENS therapy and NMES placebo therapy were given, and then NMES therapy and TENS placebo therapy were given at an interval of 30 minutes. The patients were treated once

Sponsors

Shenzhen Hospital of Beijing University of Chinese Medicine (Longgang)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? Meets the diagnostic criteria of Western medicine; ? The onset time is 1 week to 6 months, with no history of treatment; ? NRS (pain numerical score)>3 points; ? Unilateral numbness of fingers; ? Age: 18-60 years old; ? Sign an informed consent form.

Exclusion criteria

Exclusion criteria: ? Individuals with a history of neck injury, surgery, skin damage, infection, or coagulation dysfunction; ? Severe dysfunction of important organs such as the heart and lungs; ? Patients with neck tumors, tuberculosis, cervical instability, and cervical spondylotic myelopathy; ? Being in lactation or pregnancy; ? Individuals with localized metallic objects that cannot be treated; ? Unable to cooperate.

Design outcomes

Primary

MeasureTime frame
Scoring of Tanaka Yasuhisa Cervical Spondylosis Symptom Scale;

Secondary

MeasureTime frame
Neck Disabilitv Index;Pittsburgh Sleep Quality Index;

Countries

China

Contacts

Public ContactZhonglin Li

Shenzhen Hospital of Beijing University of Chinese Medicine (Longgang)

425563783@qq.com+86 137 1700 5547

Outcome results

None listed

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