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.
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…
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