Skip to content

Optical Stimulation in Peripheral Nerves for Select Rhizotomy Procedures

Optical Stimulation in Peripheral Nerves in Selective Rhizotomy Cases

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00575536
Acronym
Rhizotomy
Enrollment
19
Registered
2007-12-18
Start date
2006-01-31
Completion date
2017-11-30
Last updated
2018-05-01

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

Conditions

Spasticity

Keywords

spasticity, rhizotomy, surgery

Brief summary

The purpose of this study is to determine the safe and effective levels of optical stimulation in peripheral nerves of humans otherwise undergoing nerve lesioning in surgery.

Detailed description

The purpose of this study is to determine the safe and effective levels of optical stimulation in peripheral nerves of humans otherwise undergoing nerve lesioning in surgery, namely children undergoing selective rhizotomy for treatment of medically refractory spasticity.

Interventions

PROCEDURERhizotomy for children with spasticity

Optical Stimulation versus electrical stimulation in children who need Rhizotomy Surgery for spasticity

Sponsors

Vanderbilt University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Children over the age of 3 and younger than 17 years * Children who have failed appropriate medical therapy and are recommended for selective rhizotomy to treat spasticity by the pediatric neurosurgeon * Children who would normally undergo electrodiagnostic testing including EMG monitoring for physiologic testing during surgery * Surgery must be performed at the Vanderbilt University Children's Hospital

Exclusion criteria

* Patients in which a segment of the nerve (up to 2cm) cannot likely be identified at the time of surgery as determined by the pediatric neurosurgeon * Children not undergoing routine selective rhizotomy for medically refractory spasticity as determined by the pediatric neurosurgeon * Children who are medically unstable to tolerate an additional 20 minutes of experimental testing during the surgery * Women who are pregnant will be excluded from this study

Design outcomes

Primary

MeasureTime frame
A brief series of optical versus electrical stimulation of the nerve will be used to measure the efficacy of optical stimulation4 hours

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026