Improving Pelvic Rehabilitation Using Epidural Stimulation After Spinal Cord Injury

Recruiting N/A Interventional Study
Spinal Cord Injuries Neuromodulation Neurogenic Bladder Neurogenic Bowel Neurogenic Detrusor Overactivity
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
University College, London · Other
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About This Trial
The investigators will recruit up to 20 volunteers with chronic, supra-sacral SCI. Following screening, eligible participants will enter 'Phase I', they will complete baseline outcome measures and then have the epidural spinal cord stimulator (eSCS) implanted with either percutaneous or paddle electrodes. Preoperative and intraoperative testing will determine exact location of electrodes. Mapping…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Spinal Cord Injury (supra-sacral) * AIS A-D * \>18 years; * SCI sustained \>12 months ago; * Neurogenic detrusor overactivity (NDO) confirmed on urodynamics; * Responsive to dorsal genital nerve stimulation * Willing and able to provide informed consent * Stable medical, physi…
Contacts

Lynsey Duffell, PhD

0208 385 3787

l.duffell@ucl.ac.uk

CONTACT

Hannah Houliston, PhD

02039470291

hannah.houliston@nhs.net

CONTACT