Skip to content

The Effect of Hypercapnia on Physiological Parameters During Short-term Breathing

The Effect of Hypercapnia and Hypoxia on Physiological Parameters During Short-term Breathing Experiment

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05441007
Acronym
HYPERCO
Enrollment
15
Registered
2022-07-01
Start date
2022-06-22
Completion date
2024-06-30
Last updated
2026-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Output, High, Hypercapnia, Hypoxia

Keywords

Cardiac Output, Perfusion index, Pulse oximetry

Brief summary

The aim of the project is to evaluate the effect of hypercapnia on physiological parameters in a healthy person during short-term hypoxia and hypercapnia.

Detailed description

Hypercapnia causes changes in physiological parameters at various levels throughout the body. The study aims to evaluate the effect of hypercapnia on physiological parameters in a healthy person during short-term hypoxia and hypercapnia. It is an intervention prospective study that will be conducted at the Faculty of Biomedical Engineering on healthy volunteers. All the volunteers undergo three different phases in random order. The individual phases differ in the breathed mixture of oxygen, nitrogen and carbon dioxide gases. Non-invasive measurements of physiological parameters, especially blood oxygen saturation, perfusion index and cardiac output, will be performed continuously during the experiment.

Interventions

OTHERHypoxic

Hypoxic gas mixture Gas mixture of 10% O2 and 90% N2 for six minutes.

OTHERHypercapnic

Hypercapnic gas mixture Gas mixture of 21% O2, 5% CO2 74% N2 for six minutes.

OTHERHypoxic and Hypercapnic

Hypoxic and Hypercapnic gas mixture Gas mixture of 10% O2, 5% CO2 85% N2 for six minutes.

Sponsors

Czech Technical University in Prague
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Masking description

The participant undergoes all three phases of the experiment and the participant does not know which one is it.

Intervention model description

Interventional single blinded randomized crossover prospective study. All participants go through all study arms, in random order.

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy volunteers

Exclusion criteria

* pregnancy * severe cardiovascular conditions * severe asthma or other severe respiratory conditions * injury to the upper limbs or hands that could affect the peripheral perfusion * diabetes * hypotension or hypertension

Design outcomes

Primary

MeasureTime frameDescription
Changes in Cardiac output due to the induced hypoxia and hypercapnia1 hourBased on the induced hypoxia, hypercapnia or combination of hypoxia and hypercapnia, Cardiac output will change
Changes in Perfusion index due to the induced hypoxia and hypercapnia1 hourBased on the induced hypoxia, hypercapnia or combination of hypoxia and hypercapnia, Perfusion index will change

Countries

Czechia

Contacts

PRINCIPAL_INVESTIGATORKarel Roubik, Professor

Czech Technical University in Prague

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026