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The Pre-acclimatization Augmented Extreme Altitude Expedition (PRAGMAX)

Primary Purpose

Altitude Hypoxia, Perfusion; Complications

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Nitrogen tent preacclimatization to high altitude
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Altitude Hypoxia focused on measuring Microcirculation, Oxygen delivery capacity, Preacclimatization, nitrogen concentration tent

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy
  • Active alpinists (active alpinists denotes individuals with regular experience in alpine high mountain climbing in rock, ice and snow terrain of difficulty WS - ZS according to the Swiss Alpine Club (SAC-CAS) grading scale assessed in a self-reporting questionnaire
  • age > 18 years

Exclusion Criteria:

  • history of high-altitude pulmonary edema or cerebral edema
  • pregnancy or lactation
  • heart failure (AHA Stage B and above)
  • pulmonary hypertension
  • pulmonary disease excluding mild bronchial asthma
  • chronic kidney failure (KDIGO Stage 1 and above)
  • chronic liver disease
  • subjects with a history of smoking (> 5 PY), and high familiar predisposition for cardiovascular disease, when combined with smoking

Sites / Locations

  • University Hospital of ZurichRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Preacclimatization group

Control group

Arm Description

The participants assigned to the preacclimatization group will undergo a defined preacclimatization program by sleeping in a nitrogen concentration tent prior to an expedition to high altitude.

The participants assigned to the control group sleep in their regular environment without use of a nitrogen concentration tent prior to an expedition to a high altitude expedition.

Outcomes

Primary Outcome Measures

Difference in sublingual total capillary vessel density (TVD) induced by preacclimatization and high-altitude exposure (change from baseline)
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Difference in sublingual functional capillary density (FCD) induced by preacclimatization and high-altitude exposure (change from baseline)
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Difference in sublingual red blood cell velocity (RBCv) induced by preacclimatization and high-altitude exposure (change from baseline)
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Difference in sublingual capillary hematocrits (cHct) induced by preacclimatization and high-altitude exposure (change from baseline)
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Difference in sublingual Tissue red blood cell perfusion (tRBCp) induced by preacclimatization and high-altitude exposure (change from baseline)
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)

Secondary Outcome Measures

Change in acute mountain sickness (Lake Louise score)
Efficacy of the nitrogen concentration tent for high altitude preacclimatization by means of incidence and severity of acute mountain sickness (LLS-AMS score)
Summit success
Efficacy of nitrogen concentration tent for high altiude preacclimatization by means of incidence and severity of summit success
Nitrogen tent
Proportion of preacclimatization time in the nitrogen concentration tent within the target environmental oxygen partial pressure within a 5% boundary
Low hemoglobin oxygen saturation
Proportion of preacclimatization time with a hemoglobin oxygen saturation below 90%
Hemoglobin oxgen saturation dips
Occurrence of dips in hemoglobin oxygen saturation below 80% for >5 min during preacclimatization

Full Information

First Posted
August 3, 2022
Last Updated
August 23, 2022
Sponsor
University of Zurich
Collaborators
Swiss Sportclinic Bern
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1. Study Identification

Unique Protocol Identification Number
NCT05517044
Brief Title
The Pre-acclimatization Augmented Extreme Altitude Expedition
Acronym
PRAGMAX
Official Title
The PRe-Acclimatization auGmented extreMe Altitude eXpedition (PRAGMAX) Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 4, 2022 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
Collaborators
Swiss Sportclinic Bern

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to investigate the effect of pre-acclimatization in a nitrogen tent at home, ventilated with a slightly increased nitrogen percentage, in preparation for an expedition at extreme altitude. Specifically, the current study aims to gather knowledge, whether pre-acclimatization, first, leads to improved capillary function during an expedition to extreme altitude, and second, affects incidence of altitude sickness and the likelihood of reaching the expedition destination without oxygen supplementation. The project will be carried out in two phases corresponding to two randomized controlled trials in healthy volunteers, who are participating in an expedition at extreme altitudes with or without pre-acclimatization.
Detailed Description
Expeditions to the world's highest peaks are attempted by increasing numbers of alpinists, taking advantage of broad commercial support. At extreme altitude successful functioning, and even survival, are only possible with adequate acclimatization, which consists of time-consuming exposure to gradually higher sleeping altitudes. Generally, an increase in 300-600 m per day at altitudes above 3000 m, and the minimization of cumulative time spend above 6500 m, are considered safe practice. Mainly in an attempt to accelerate expeditions to extreme altitudes, a preacclimatization technique using nitrogen concentration tent induced normobaric hypoxia is increasingly employed in practice, and already part commercial expedition plans. Some previous research indicates that intermittent normobaric hypoxia may reduce the incidence of acute mountain sickness, while the results from other studies remain inconclusive or negative. One study has not found serious adverse effects related to intermittent normobaric hypoxia, such as high-altitude pulmonary or cerebral edema. Thus, despite the emergence of increasing numbers of commercial expedition programs making use of nitrogen concentration tent preacclimatization protocols, many factors remain unclear. Next to remaining uncertainties regarding the extent of the hypoxic condition induced by these devices, current data does not allow adequate conclusions regarding the choice of optimal preacclimatization protocol, optimal associated ascent profiles, and possible effects on oxygen delivery capacity to the tissue, incidence of high-altitude related disease, and even summit success. Thus, the present study aims to conduct a randomized controlled trial to assess the efficacy of nitrogen concentration tent preacclimatization as part of two expeditions to extreme altitude. The immediate effects of nitrogen concentration tent preacclimatization are assessed through continuous monitoring of oxygen partial pressure in the tent and the hemoglobin oxygen saturation throughout preacclimatization. To test whether preacclimatization is associated with physiologic adaptation, tissue red blood cell perfusion as a main contributor to increase oxygen delivery capacity in the microcirculation throughout acclimatization to extreme altitude, is assessed using non-invasive handheld vital microscopy during preacclimatization and throughout the expedition, and the incidence and severity of high-altitude related disease and summit success, are recorded during the expeditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Altitude Hypoxia, Perfusion; Complications
Keywords
Microcirculation, Oxygen delivery capacity, Preacclimatization, nitrogen concentration tent

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Two independent randomized-controlled trials with each an intervention and a control group.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Preacclimatization group
Arm Type
Experimental
Arm Description
The participants assigned to the preacclimatization group will undergo a defined preacclimatization program by sleeping in a nitrogen concentration tent prior to an expedition to high altitude.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
The participants assigned to the control group sleep in their regular environment without use of a nitrogen concentration tent prior to an expedition to a high altitude expedition.
Intervention Type
Other
Intervention Name(s)
Nitrogen tent preacclimatization to high altitude
Intervention Description
The participants assigned to the preacclimatization group spend a minimum of six hours during sleep, throughout the acclimatization period (four weeks preceding the expedition) in a nitrogen concentration tent (Hypoxico OHG, Traunstein, Germany) set to an environmental PO2 corresponding to an altitude of 2500 masl, with a progression to 5500 masl within 28 days in steps of 1000 m every seven days. Respiratory Polygraphy is used to detect periodic breathing, SpO2, and heart rate continuously during sleep and is performed before and after the designated preacclimatization period, and repetitively when increasing normobaric hypoxia in the group with nitrogen concentration tent preacclimatization.
Primary Outcome Measure Information:
Title
Difference in sublingual total capillary vessel density (TVD) induced by preacclimatization and high-altitude exposure (change from baseline)
Description
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Time Frame
Microcirculation assessment taken: 4 and 1 week prior to the expedition start (preacclimatization), Day 5 to 10 of the expedition in Nepal, Day 2 after the return from Nepa
Title
Difference in sublingual functional capillary density (FCD) induced by preacclimatization and high-altitude exposure (change from baseline)
Description
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Time Frame
Microcirculation assessment taken: 4 and 1 week prior to the expedition start (preacclimatization), Day 5 to 10 of the expedition in Nepal, Day 2 after the return from Nepa
Title
Difference in sublingual red blood cell velocity (RBCv) induced by preacclimatization and high-altitude exposure (change from baseline)
Description
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Time Frame
Microcirculation assessment taken: 4 and 1 week prior to the expedition start (preacclimatization), Day 5 to 10 of the expedition in Nepal, Day 2 after the return from Nepa
Title
Difference in sublingual capillary hematocrits (cHct) induced by preacclimatization and high-altitude exposure (change from baseline)
Description
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Time Frame
Microcirculation assessment taken: 4 and 1 week prior to the expedition start (preacclimatization), Day 5 to 10 of the expedition in Nepal, Day 2 after the return from Nepa
Title
Difference in sublingual Tissue red blood cell perfusion (tRBCp) induced by preacclimatization and high-altitude exposure (change from baseline)
Description
Sublingual microcirculatory functional hemodynamic variable measured using a handheld vital microscopy. (ref: Communications Biology 2019; 2: 217 UND ref. Curr Opin Crit Care 2020; 26: 273-280.)
Time Frame
Microcirculation assessment taken: 4 and 1 week prior to the expedition start (preacclimatization), Day 5 to 10 of the expedition in Nepal, Day 2 after the return from Nepa
Secondary Outcome Measure Information:
Title
Change in acute mountain sickness (Lake Louise score)
Description
Efficacy of the nitrogen concentration tent for high altitude preacclimatization by means of incidence and severity of acute mountain sickness (LLS-AMS score)
Time Frame
LLS_AMS score reported: 4 and 1 week prior to the expedition start (preacclimatization), Day 5 to 10 of the expedition in Nepal, Day 2 after the return from Nepal
Title
Summit success
Description
Efficacy of nitrogen concentration tent for high altiude preacclimatization by means of incidence and severity of summit success
Time Frame
Day 9 of the expedition in Nepal (Summit attempt)
Title
Nitrogen tent
Description
Proportion of preacclimatization time in the nitrogen concentration tent within the target environmental oxygen partial pressure within a 5% boundary
Time Frame
4 weeks (prior to the expedition start (preacclimatization))
Title
Low hemoglobin oxygen saturation
Description
Proportion of preacclimatization time with a hemoglobin oxygen saturation below 90%
Time Frame
4 weeks (prior to the expedition start (preacclimatization))
Title
Hemoglobin oxgen saturation dips
Description
Occurrence of dips in hemoglobin oxygen saturation below 80% for >5 min during preacclimatization
Time Frame
4 weeks (prior to the expedition start (preacclimatization))

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy Active alpinists (active alpinists denotes individuals with regular experience in alpine high mountain climbing in rock, ice and snow terrain of difficulty WS - ZS according to the Swiss Alpine Club (SAC-CAS) grading scale assessed in a self-reporting questionnaire age > 18 years Exclusion Criteria: history of high-altitude pulmonary edema or cerebral edema pregnancy or lactation heart failure (AHA Stage B and above) pulmonary hypertension pulmonary disease excluding mild bronchial asthma chronic kidney failure (KDIGO Stage 1 and above) chronic liver disease subjects with a history of smoking (> 5 PY), and high familiar predisposition for cardiovascular disease, when combined with smoking
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthias P Hilty, PD Dr. med.
Phone
+41 43 253 8063
Email
matthias.hilty@usz.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Jacqueline Pichler Hefti, PD Dr. med.
Phone
+41 32 324 24 24
Email
jacqueline.pichler@szb-chb.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthias P Hilty, PD Dr. med.
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthias Hilty, PD. Dr. med.
Phone
+41 43 253 80 63
Email
matthias.hilty@usz.ch

12. IPD Sharing Statement

Plan to Share IPD
No

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The Pre-acclimatization Augmented Extreme Altitude Expedition

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