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
Group Intervention Description Bilateral rapid magnetic stimulation of the phrenic nerves Magnetic phrenic nerve stimulation Each 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
Name Time Method Diaphragm contractility Continuously 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
Name Time Method
Trial Locations
- Locations (1)
Exercise Physiology Lab, Institute of Human Movement Sciences and Sport, ETH Zurich
🇨ðŸ‡Zurich, ZH, Switzerland