About this trial
Procedural pain is inadequately managed in two-thirds of patients undergoing invasive medical procedures. Several techniques exist for managing procedural pain, but they all present implementation challenges and are not without side effects. Therefore, a new, non-pharmacological, inexpensive, and easy-to-use approach would be of significant benefit. Transcutaneous electrical nerve stimulation (TENS) for pain relief could represent this alternative. Few studies have been conducted on the benefits of TENS in managing procedural pain, for example, in shoulder arthrodistension. This project proposes to study it in the context of posterior ramus infiltration in patients eligible for this indication, in the context of chronic low back pain associated with posterior joint syndrome.
Eligibility criteria
Qualifiers
Chronic low back pain (lasting more than 3 months)
Patient followed in a Chronic Pain Unit (CETD, Toulouse University Hospital)
Clinical and radiological diagnosis (CT scan or MRI) of posterior joint syndrome
Patient with an indication for infiltration therapy, feasible under standard conditions
Disqualifiers
Spinal surgery
Wearing an electronic medical device (pacemakers, defibrillators, etc.)
Pregnancy
Area of cutaneous anesthesia
Trial design
Treatments tested in this trial
- Stimulation with TENS, which allows the release of endorphins
- Stimulation with TENS does not allow the release of endorphins
- Questionnaires