Skip to main content
Clinical Trials/NCT01468194
NCT01468194
Completed
Not Applicable

Change in Peripheral Oxygen Saturation by Using Different Breathing Procedures in High Altitude

University of Giessen1 site in 1 country30 target enrollmentJuly 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Mountain Sickness
Sponsor
University of Giessen
Enrollment
30
Locations
1
Primary Endpoint
change of peripheral oxygen saturation
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

In this investigation the researchers explore whether different types of breathing procedures can improve the peripheral oxygen saturation to reduce the risk of becoming a acute mountain sickness or a high altitude pulmonary edema.

Detailed Description

Acute mountain sickness (AMS) is a pathological effect of high altitude on humans caused by acute exposure to low partial pressure of oxygen at high altitude. It commonly occurs above 2500 meters of altitude. AMS appears as a collection of nonspecific symptoms acquired at high altitude or in low air pressure resembling a case of "flu, carbon monoxide poisoning, or a hangover". It is caused by a drop in pressure and lowering partial pressure of oxygen during increasing altitude. The direct consequence of those changes is a hypoxic pulmonary vasoconstriction (Euler-Lijestrand-mechanism). In addition a rise in pulmonary blood pressure (Hypertonia) can occur so that there is a higher risk of developing a high altitude pulmonary edema (HAPE). In this investigation the investigators are exploring whether different types of breathing procedures can improve the peripheral oxygen saturation. We are comparing breathing with no regulation with two different procedures of hyperventilation during trekking in different altitudes. Procedure 1 (hyperventilation 1) describes inhalation during one step and exhalation during the next step. Procedure 2 (hyperventilation 2) describes inhalation and exhalation during one step. The effect of the different breathing procedures can be quantified measuring the peripheral oxygen saturation. In addition the investigators are comparing the breathing rate and the minute ventilation as well as the expiratory end-tidal CO2-partial pressure of the three different breathing procedures. Furthermore, the investigators are examining the ability to concentrate in order to quantify the effect of AMS on organ functions.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
November 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Andree Hillebrecht

Akademischer Rat

University of Giessen

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • acute clinically significant inter-current diseases

Outcomes

Primary Outcomes

change of peripheral oxygen saturation

Time Frame: immediate after intervention

change of peripheral oxygen saturation under different breathing procedures in different altitudes

Secondary Outcomes

  • change of breathing parameters(immediate after intervention)
  • change of cognition(immediate after intervention)

Study Sites (1)

Loading locations...

Similar Trials