Effects of Blood Gas Perturbations

ConditionHealthy
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-55
SponsorSwiss Federal Institute of Technology

About this trial

In this study, the effects of blood gas perturbations on neuromuscular function of the diaphragm and lower limbs at rest and during exercise will be investigated.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

healthy

non.smoking

normal lung function

BMI: 18.5-29.9 kg/m2

Disqualifiers

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

Trial design

Design model

Single group

Treatments tested in this trial

  • Gas perturbation

    Other intervention

    Participants will be breathing a gas mixture of either room air, or hypoxia, or hypercapnia, or a combination of both during 2h. This is followed by an all-out breathing exercise test against a small resistance, while still being in the respective gas condition.

Treatment groups

16 Participants
are divided into 1 treatment group
Group A: Gas perturbationsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Diaphragm contractility

Diaphragm contractility measured before/during/following the gas exposures and the volitional respiratory muscle exercises using transdiaphragmatic and mouth pressure responses.

Time frame
Continuously measured from 10 sec before until 10 sec after each stimulation. One stimulation lasts for approx. 1 sec

Secondary outcomes

Other outcomes

1

Quadriceps contractility

Quadriceps contractility will be assess before, during and following the gas exposures and respiratory muscle contractions

Time frame
Continuously measured from 10 sec before until 10 sec after each stimulation. One stimulation lasts for approx. 1 sec.

Locations

This trial has no locations.

Sponsors and contacts

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