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Functional Changes in the Brain After Tibial Nerve Stimulation: a Pilot Study

S

Swiss Paraplegic Research, Nottwil

Status

Completed

Conditions

Spinal Cord Injuries
Bladder, Neurogenic

Treatments

Other: magnetic resonance imaging

Study type

Observational

Funder types

NETWORK

Identifiers

NCT03908047
2019-01

Details and patient eligibility

About

The lower urinary tract is innervated by the autonomous (sympathetic, parasympathetic) and the somatic nervous system. Afferent information from the lower urinary tract (LUT) (e.g. filling state and volume of the urinary bladder) is conducted via the dorsal roots to the sacral spinal cord and from there to the pontine micturition center (PMC) in the brain stem. The PMC has several connections to other cortical areas. These complex interactions with the cortex enable voluntary control of the LUT and are crucial for urinary continence. The integrity of this neuronal circuit is crucial for an undisturbed function. Deterioration of the nerve fibers due to a systemic neurological disease (e.g. spinal cord injury) can affect LUT function. Neurogenic lower urinary tract dysfunction can lead to urgency, urge incontinence, reduced bladder capacity and secondary deterioration of the upper urinary tract (i.e. kidneys). First-line therapy of neurogenic detrusor overactivity contains antimuscarinic treatment. In case of side effects or remaining detrusor overactivity, nerve stimulation (e.g. sacral neuromodulation and in effect nerve tibialis stimulation) is an accepted therapy option. The precise mechanism of action of these neuro-modulatory procedures is still unknown. Utilizing state-of-the-art neuroimaging techniques, we intend to investigate the functional activation pattern after afferent tibialis nerve stimulation as well as the association with the architecture of the sacral roots. We aime to get a better insight into functional neuromodulation and central nervous processing. The study aim is to evaluate the feasibility in healthy subjects as a pilot study for the application of these method in patients with chronic, incomplete spinal cord injury.

Enrollment

15 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy volunteers
  • 18-50 years old
  • informed consent

Exclusion criteria

  • history of neurological disease (eg. multiple sclerosis, epilepsy)
  • cardiac pacemaker, insulin or other pumps
  • claustrophobia
  • pathological findings in the uroflowmetry or post void residual assessment
  • medication with central nervous effects
  • pregnancy or lactating
  • unable to give informed consent

Trial design

15 participants in 1 patient group

healthy volunteers
Treatment:
Other: magnetic resonance imaging

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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