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Frequency and Pulse Duration Programming in Spinal Cord Stimulation

An Observational Study of the Effect of Frequency and Pulse Duration Programming on Paresthesia Perception in Spinal Cord Stimulation for Low Back Pain

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12611001118998
Enrollment
40
Registered
2011-10-26
Start date
2012-02-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

In this study we seek to investigate the effect of varying pulse width and frequency on paresthesia perception. This study seeks to confirm the findings of Yearwood et al (2007, 2010) that varying pulse width can shift the focus of paresthesia and to provide the first findings on the effect of frequency on paresthesia perception. In addition, we will report on the interaction between pulse width and frequency changes.

Interventions

Obervation of the effect of the varying pulse duration and frequency on paresthesia perception. Participants are observed for several hours on one day only. The whole study is expected to be completed in 9 months.

Sponsors

Dr Marc Russo
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients implanted with Precision Spinal Cord Stimulator (SCS) system for > 3 months Epidural lead(s) implanted between T6 and T12 for chronic neuropathic pain of the trunk or limbs Ability to use tablet pen to draw paresthesia coverage on computer graphics program Capable of giving written consent and willingness to comply with study procedures

Exclusion criteria

Other major pain area not targeted by Spinal Cord Stimulator (SCS) system Potential for further surgery: Spinal Cord Stimulator (SCS) revision, other surgery for pain Other medical condition likely to interfere with study procedures or likely to confound evaluation of endpoints Currently unable to use the device due to device problems or other medical conditions Pregnancy

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026