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Peripheral Nerve Activation Sensitivity (PERNEAC)

T

Thomas Niederhauser

Status

Enrolling

Conditions

Nerve Excitation Sensitivity

Treatments

Device: Electric and electromagnetic stimulation

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT07160413
108.018 IP-LS (Other Grant/Funding Number)
2025-00776

Details and patient eligibility

About

Volunteers will undergo various peripheral nerve stimulations (electric, electromagnetic, and temporal interference) to evaluate each method's sensitivity. The main objective is to examine the relationship between nerve activation and coil placement relative to the nerve, as well as how different coil types influence maximal nerve activation.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Person aged > 18 years
  • Signed informed consent
  • Healthy
  • Willingness and ability to adhere to study procedures

Exclusion criteria

  • Known hypersensitivity to electric or electromagnetic stimulation
  • Any implanted metal or electronic device in the upper body (except dental work such as fillings or braces), e.g., active medical devices, metal implants
  • Neurological or neuromuscular disorders or conditions
  • History of seizures or epilepsy
  • Current treatment with drugs that lower seizure threshold (e.g., certain analgesics, methylxanthines, antipsychotics, antidepressants, antiepileptics, anesthetics)
  • Pregnancy or breastfeeding
  • Surgical intervention of the arm within the last 4 weeks
  • Allergy to adhesives or ultrasound gel components (e.g., polyethylene glycols)
  • Skin lesions, infections, or strictures in the arm region
  • Tattoos on the stimulated (right) arm and hand, or in any area likely to be captured in video recordings
  • Inability to follow study procedures (e.g., due to language barrier, psychological disorders, dementia)
  • Participant deprived of liberty by administrative or judicial decision or under legal guardianship

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Stimulated
Experimental group
Treatment:
Device: Electric and electromagnetic stimulation

Trial contacts and locations

1

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Central trial contact

Thomas Niederhauser, PhD

Data sourced from clinicaltrials.gov

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