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Snow Properties and Its Modeling for Studying Gas Exchange Under the Simulated Avalanche Snow

Snow Properties and Its Modeling for Studying Gas Exchange Under the Simulated Avalanche Snow

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03413878
Acronym
SPAM
Enrollment
45
Registered
2018-01-29
Start date
2018-01-29
Completion date
2022-05-20
Last updated
2021-02-25

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

Conditions

Accident Caused by Snow Avalanche

Keywords

snow, avalanche, hypercapnia, work of breathing

Brief summary

The aim of the study is to investigate respiratory parameters of a person in the simulated avalanche snow and consequent use of the measured data for development of a mathematical-physical model of breathing during increasing hypercapnia in the avalanche.

Detailed description

The study is a part of a university research project aimed at studying physiological conditions and development of breathing parameters of a person breathing in the simulated avalanche snow. Presence of an air pocket and its size play an important role in survival of victims buried in the avalanche snow. Even small air pockets facilitate breathing, yet they do not provide a significant amount of fresh air for breathing. The investigators hypothesize that the size of the air pocket significantly affects the airflow resistance and work of breathing. The aim of the study is to investigate the effect of the air pocket volume on gas exchange and work of breathing in subjects breathing into the simulated avalanche snow.

Interventions

OTHERBreathing in the simulated avalanche snow

Breathing in the simulated wet or dry avalanche snow with a small or large air pocket

Sponsors

Charles University, Czech Republic
CollaboratorOTHER
Ministry of Defence and Armed Forces of the Czech Republic
CollaboratorUNKNOWN
Czech Technical University in Prague
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy and fit volunteers, classified as The American Society of Anesthesiologists class I * without a smoking history

Exclusion criteria

* Tiffeneau Index less than 0.70 * any cardiovascular or respiratory condition

Design outcomes

Primary

MeasureTime frameDescription
The length of breathingContinuously within 30 minute interval from the beginning of the breathing experimentTime to termination of the breathing experiment due to the decision of the tested subject, or determined by high end-tidal carbon dioxide value or by the order by the clinician assessing the health status of the subjects.

Countries

Czechia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026