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Combined radiofrequency ablation and pulsed neuromodulation to treat cervical facet joint pain alleviate post cervical radiofrequency side effects

Combinded continuous radiofrequency ablation and pulsed neuromodulation to treat cervical facet joint pain alleviate post cervical radiofrequency side effects

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20221015001
Enrollment
39
Registered
2022-10-15
Start date
2014-06-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Continuous radiofrequency ablation followed by pulsed neuromodulation to treat cervical facet joint pain alleviate post cervical radiofrequency complication cervical facet joint pain, combined radiofrequency, continuous radiofrequency, facet joint injection, medial branch blocks, neck pain, pulse radiofrequency, radiofrequency ablation, radiofrequency neurotomy

Interventions

Continuous radiofrequency ablation for 80 degree Celsius for 90 sec ,2 cycle,Continuous radiofrequency ablation for 80 degree Celsius for 90 sec , 1 cycle followed by pulsed neuromodulation 42 degree
Active Comparator Procedure/Surgery,Experimental Procedure/Surgery
Continuous radiofrequency ablation,Continuous radiofrequency ablation followed by pulsed neuromodulation

Sponsors

Phramongkutklao Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who presented positive diagnostic cervical medial braches block defined as pain relief more than 50%from baseline

Exclusion criteria

Exclusion criteria: Patients who repeated cervical radiofrequency ablation, patients presenting neck pain with radicular symptoms,malignancy, psychological problem, language barrier, history of allergy to radio-opaque contrast solution, lidocaine or bupivacaine and inadequate medical records.

Design outcomes

Primary

MeasureTime frame
Successful treatment At least 3 months Visual analog scale (VAS) expressed as at least 80% pain relief from baseline and NDI score less than 15

Secondary

MeasureTime frame
Post radiofrequency side effects Post radiofrequency peroid Side effects including numbness, ataxia, dysesthesia, hypersensitivity, itching and muscular weakness (dropped head syndrome)

Countries

Thailand

Contacts

Public ContactSithapan Munjupong

Phramongkutklao Hospital

sithapan@gmail.com0991959255

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026