Trials / Terminated
TerminatedNCT02250469
A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthesia Between 2 Spinal Cord Stimulation Systems
A Randomised Pilot Study to Assess differenCes in tHe Subjects' Experience of stimulAtion-Induced paRaesthesiA Between Two Different Spinal Cord sTimulation dEvices: the Axium® DoRsal Root Ganglion Stimulation System Versus the Prime Advanced Dorsal Column Stimulation System
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 5 (actual)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
12-SMI-2014 is a post-market, randomised, pilot study to identify and rate differences in patient experiences with two different types of Spinal Cord Stimulator devices which are routinely used to treat chronic pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Treatment with the Axium SCS system | |
| DEVICE | Treatment with the Medtronic SCS System |
Timeline
- Start date
- 2014-09-01
- Primary completion
- 2016-12-01
- Completion
- 2016-12-01
- First posted
- 2014-09-26
- Last updated
- 2022-11-09
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT02250469. Inclusion in this directory is not an endorsement.