High-Voltage Pulsed Radiofrequency of the Lumbar Dorsal Root Ganglion for the Treatment of Chroni… (NCT06264297) | Clinical Trial Compass
RecruitingNot Applicable
High-Voltage Pulsed Radiofrequency of the Lumbar Dorsal Root Ganglion for the Treatment of Chronic Lumbar Radicular and Neuropathic Pain; A Prospective, Doble-blinded and Randomized Controlled Trial
Spain98 participantsStarted 2023-02-20
Plain-language summary
The management of chronic lumbar radicular and neuropathic pain is complex and the treatment success rates are low. Pulsed radiofrequency (PRF) has been described in these cases. In order to determine whether high-voltage PRF show better results than PRF a prospective, doble-blinded and randomized study is conducted in patients with chronic lumbar radicular and neuropathic pain.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients over 18 years of age.
* Unilateral pain radiating to the lower extremity (with or without lumbar pain), which clinically corresponds to the path of the corresponding dermatomes.
* Correlation between clinical symptoms and lesion observed by magnetic resonance imaging (MRI).
* Radicular syndrome of three months or more of evolution.
* Normal or pathological electromyogram (EMG).
* Pain with neuropathic characteristics confirmed by the DN4 neuropathic pain questionnaire.
* Patients with a previous positive block diagnosis.
* Patients who have signed the informed consent document.
Exclusion Criteria:
* Patients under 18 years of age.
* Patients with non-radicular low back pain.
* MRI not consistent with the patient\'s symptoms.
* Patients with peripheral neuropathy of the lower extremities.
* Patients with a history or current diagnosis of serious mental disorder.
* Patients with moderate or severe cognitive impairment, or evidence of acute or subacute confusional syndrome.
* Infection at the puncture site.
* Coagulation disorders.
* Pregnant patients.
* Patients who refuse to sign the informed consent document.
* Patients allergic to radiological contrast.
What they're measuring
1
OSWESTRY LOW BACK DISABILITY QUESTIONNAIRE
Timeframe: From enrollment to the end of treatment at 6 months