Skip to content

Ultrasound-guided low-temperature plasma radiofrequency ablation for cervical disc herniation: a clinical comparative study

Ultrasound-guided low-temperature plasma radiofrequency for the treatment of cervical disc herniation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021417
Enrollment
Unknown
Registered
2019-02-20
Start date
2019-02-25
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

Cervical spondylopathy

Interventions

Group 1:Ultrasound-guided low-temperature plasma radiofrequency therapy
Group 2:Ultrasound-guided radiofrequency thermocoagulation therapy

Sponsors

The First Hospital of Harbin City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Conformity with the clinical diagnostic criteria of cervical spondylosis; (2) Magnetic resonance imaging (MRI) proved that cervical spondylosis had no prolapse or dissociation of the disc, no history of cervical surgery, no calcification or fragmentation of the cervical disc, no cervical segmental instability, no osteogenic spinal stenosis; (3) persistent neck and shoulder soreness or root pain; (4) patients had not received any other symptoms in the recent six months. Conservative or non-surgical treatment; (5) The patient agrees to participate in the trial and is willing to follow up for a long time after operation, and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Cervical and shoulder pain caused by other causes such as non-cervical spondylosis; (2) cervical infection or steroid allergy history; (3) patients with severe diabetes, malignant hypertension, severe heart disease and other non-low temperature plasma radiofrequency; (4) cervical disc prolapse and dissociation, cervical disc calcification or fragmentation, cervical segmental instability, bone Sexual spinal stenosis; (5) patients with poor compliance, can not cooperate with the completion of the treatment process.

Design outcomes

Primary

MeasureTime frame
Visual analog scale;

Countries

China

Contacts

Public ContactBaolin Li

The First Hospital of Harbin City

baoli09@163.com+86 18249514430

Outcome results

None listed

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