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.
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