The Potential of Transcutaneous Electrical Nerve Stimulation to Improve Pain Experienced During Posterior Branch Blocks in Patients With Lumbar Posterior Joint Syndrome

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Toulouse

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

Treatment groups

52 Participants
are divided into 2 treatment groups

Sponsors and collaborators