Transcutaneous Spinal Stimulation for Children and Youth With Spina Bifida

Recruiting N/A Interventional Study
Myelomeningocele Spina Bifida
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
5 – 18
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
30 (estimated)
Sponsor
Mayo Clinic · Other
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About This Trial

A study to use transcutaneous spinal cord stimulation to characterize sensorimotor deficits in a pediatric population of individuals with spina bifida.

Trial Locations
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Eligibility Criteria
Inclusion Criteria * Congenital diagnosis of myelomeningocele (MMC) * Able to follow verbal commands or instructions. * If female and able to become pregnant, must be willing to use medically-acceptable method of contraception during study participation. Exclusion Criteria * Severe cognitive defi…
Contacts

Julie Block

507-255-7393

Block.Julie@mayo.edu

CONTACT