GasProp: Evaluation of Gas Propagation in Snow During Breathing of Subjects Under Simulated Avalanche Snow

Sponsor
Czech Technical University in Prague (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05262894
Collaborator
(none)
50
1
1
39.7
1.3

Study Details

Study Description

Brief Summary

The study is aimed at investigation of respiratory gases propagation in snow. The study involves volunteers breathing into the snow whereas concentrations of gases are measured at various positions in the snow.

Condition or Disease Intervention/Treatment Phase
  • Other: extreme hypercapnia induced by ventilation insufficiency
N/A

Detailed Description

The study is aimed at investigation of respiratory gases (oxygen and carbon dioxide) propagation in the simulated avalanche snow. The study involves volunteers breathing into the snow whereas concentrations of gases are measured at various positions in the snow. A special apparatus was created for sampling and measurement of gas concentrations and to assure stable geometry of the experiment required for data evaluation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Evaluation of Gas Propagation in Snow During Breathing of Subjects Under Simulated Avalanche Snow
Actual Study Start Date :
Feb 7, 2022
Anticipated Primary Completion Date :
May 31, 2025
Anticipated Study Completion Date :
May 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Breathing in the snow

Breathing in the snow using a specially designed apparatus and measuring the respiratory gases distribution in snow.

Other: extreme hypercapnia induced by ventilation insufficiency
Re-breathing of gas by breathing into the simulated avalanche snow

Outcome Measures

Primary Outcome Measures

  1. The length of breathing [Continuously within up to 20 minute interval from the beginning of the breathing experiment]

    Time 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Czech Technical University, Faculty of Biomedical Engineering Kladno Czechia 272 01

Sponsors and Collaborators

  • Czech Technical University in Prague

Investigators

  • Principal Investigator: Karel Roubik, prof., Czech Technical University in Prague, Fac. of Biomedical Engineering

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Czech Technical University in Prague
ClinicalTrials.gov Identifier:
NCT05262894
Other Study ID Numbers:
  • 2022-Bradler
First Posted:
Mar 2, 2022
Last Update Posted:
Mar 2, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Czech Technical University in Prague

Study Results

No Results Posted as of Mar 2, 2022