None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subject should have lumbar or sacral radicular neuropathic pain in dermatome L4, L5 or S1 where the pain is limited for 1 dermatome for at least 3 month. The subject should have a pain reduction of minimum 50% with a VAS score from 0 to 10 after a diagnostic block.
Exclusion criteria
Exclusion criteria: 1. Subject has sensory deficits at the QST site resulting from such medical conditions such as diabetes, alcoholic neuropathy, AIDS neuropathy, severe thyroid, liver or kidney diseases; 2. Former PRF or RF treatment of the same nerve root; 3. Subject has scar tissue, infection or acute injury at the QST site; 4. Language barriers and other problems impairing the reliable completion of questionnaires; 5. Subject is pregnant; 6. Subject has a pacemaker; 7. Subject has a major psychiatric disease or dementia; 8. History of back surgery; 9. Other chronic pain (such as fibromyalgia); 10. Anticoagulation in form of vitamin K antagonists which should not be stopped; 11. Skin diseases (such as herpes zoster, burns etc.); 12. Allergion for contrast or lidocaine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Electrical quantitative sensory testing values before and after treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. VAS score; 2. Symptoms of pain (pain detect); 3. Medication use; 4. RAND-36 questionnaire; 5. HADS score. | — |
Contacts
Haaksbergerstraat 55, poli 30