R52.1
Conditions
Interventions
Group 1: Tonic stimulation - external tonic stimulation for 7 days
Group 2: Burst stimulation - external burst stimulation for 7 days
Sponsors
Universitätsklinikum Düsseldorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Implantation of a test lead for dorsal root ganglion stimulation trial. 2. Pain intensity of more than 5 on visual analog scale for more than 3 months. 3. The patient has the ability to read, understand and give information reliably as required by the protocol.
Exclusion criteria
Exclusion criteria: 1. Patients with another pain disorder, which could influence the study results 2. Adults unable to give consent 3. Children and adolescents
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity using the visual analog scale (VAS) at the end of the trial phases of tonic and burst stimulation | — |
Secondary
| Measure | Time frame |
|---|---|
| Life quality, analgesics intake, patient satisfaction | — |
Countries
Germany
Contacts
Public ContactGuilherme Santos Piedade
Universitätsklinikum Düsseldorf
Outcome results
None listed