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Quantification and Repeatability of Magnetic Stimulation

Not Applicable
Active, not recruiting
Conditions
Healthy
Interventions
Other: Magnetic phrenic nerve stimulation
Registration Number
NCT05302752
Lead Sponsor
Swiss Federal Institute of Technology
Brief Summary

In this project the quantification and the repeatability of responses to rapid bilateral magnetic stimulation of the phrenic nerves will be investigated in healthy humans.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
16
Inclusion Criteria
  • healthy
  • non-smoking
  • normal lung function
  • body mass index: 18.5-29.9 kg/m2
  • able to communicate in english
  • willing to adhere to study rules
Exclusion Criteria
  • acute illness or chronic conditions of the gastrointestinal tract, and health conditions affecting metabolism, the cardiovascular or the respiratory system, or sleep
  • intake of medications affecting metabolism, the cardiovascular, the neuromuscular or the respiratory system, or sleep
  • any metal or electronics inside of the body
  • presence of cardiac pacemaker, implanted defibrillators or implanted neurostimulators
  • history of seizures or epilepsy
  • tatoos on the stimulation sites
  • previous enrolment in this study
  • for women: pregnancy, breastfeeding, or intention to become pregnant during the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Bilateral rapid magnetic stimulation of the phrenic nervesMagnetic phrenic nerve stimulationEach participant will be tested on three different days with optimal settings for bilateral rapid magnetic stimulation of the phrenic nerves established on visit 1 and then repeated on visits 2 and 3.
Primary Outcome Measures
NameTimeMethod
Diaphragm contractilityContinuously measured from 10 sec before until 10 sec after each stimulation. One stimulation lasts for approx. 1 sec

Transdiaphragmatic pressure changes, i.e. changes in esophageal and gastric pressures, will be measured by a pressure transducer connected to balloon-catheters.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Exercise Physiology Lab, Institute of Human Movement Sciences and Sport, ETH Zurich

🇨🇭

Zurich, ZH, Switzerland

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