Triple H ODC Trial (3H-ODC)
Primary Purpose
Hypoxia, Hypothermia, Accidental, Hypercapnia
Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
blood sampling
Sponsored by
About this trial
This is an interventional basic science trial for Hypoxia
Eligibility Criteria
Inclusion Criteria:
- 18-40 years
- fasted situation
- ASA I
- Informed Consent
Exclusion Criteria:
- any drug abuse
- any drug intake within the last 10 days
- smoking
- known hemoglobinopathy
- relevant illness within last 14 days
- relevant blood loss within last 14 days
- pregnancy or breast-feeding
- participation in any pharmacological study
- exposure to high altitude (> 3000 m) within last 4 weeks
Sites / Locations
- General and Surgical Critical Care Medicine, Medical University of Innsbruck
Outcomes
Primary Outcome Measures
amount of p50 in different levels of hypercapnia and hypothermia
amount of p50 in mmHg (p50 = pO2 when oxygen saturation of hemoglobin is 50%)
Secondary Outcome Measures
amount of p50 shift due to sex
amount of p50 in mmHg (p50 = pO2 when oxygen saturation of hemoglobin is 50%)
amount of inflection point in different levels of hypercapnia and hypothermia
amount of inflection point in mmHg
Full Information
NCT ID
NCT04041531
First Posted
July 26, 2019
Last Updated
September 8, 2020
Sponsor
Medical University Innsbruck
Collaborators
Institute of Mountain Emergency Medicine
1. Study Identification
Unique Protocol Identification Number
NCT04041531
Brief Title
Triple H ODC Trial
Acronym
3H-ODC
Official Title
Determination of the Oxygen Dissociation Curve Under the Conditions of an Avalanche Burial With an Air Pocket
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
August 26, 2019 (Actual)
Primary Completion Date
November 30, 2019 (Actual)
Study Completion Date
February 10, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University Innsbruck
Collaborators
Institute of Mountain Emergency Medicine
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In an avalanche burial with an air pocket hypercapnia (and hypoxia) develops within few minutes, hypercapnia increases the rate of cooling and therefore the development of hypothermia. The Triple H Syndrome (Hypoxia, Hypercapnia, Hypothermia) occurs. This specific combination of the three parameters is unique for avalanche burial with an air pocket. Every single parameter has a substantial effect on the hemoglobin-oxygen dissociation curve, but until now no study described the combination of these three parameters. This curve will be measured under these specific conditions in a specifically developed in vitro model, to quantify its shifts and to show if there are combined effects of pCO2 and temperature. The newly developed method will be validated in comparison with an established method. The project will be performed with whole blood, drawn by healthy volunteers, in an experimental setting. The samples will be blinded to the investigator and analyzed in a randomized manner.
Detailed Description
The ODC is a function of pO2 and SO2. pO2, the independent variable, is plotted on the x axis, SO2 on the y axis. For the determination of this function, a pairwise measurement of pO2 and the corresponding SO2 is to be performed. Using nonlinear regression analysis, the ODC can be fitted to the measured points that describe the relation of pO2 and SO2 and characteristic parameters like p50 value and inflection points can be calculated.
To measure the ODC under the conditions of the Triple H Syndrome (Hypoxie, Hypercapnia, Hypothermia), the temperature and the pCO2 have to be changed and controlled during the measurement. No commercially available instrument is able to obtain this. Therefore, we envisaged the development of an entirely new approach.
In the 3H ODC trial venous blood will be drawn from 18 - 40 years old female and male volunteers by a unique venipuncture. The participants have to be in a fasted situation, ASA I and nonsmokers. The blood sample will be immediately pseudonymized and stored on ice and a venous blood gas analysis will be carried out (pH, Hb, COHb, MetHb, FHb). Simultaneous to the main measurement, 2,3 BPG will be quantified by an ELISA test and any unknown hemoglobinopathy will be excluded by Hemoglobin Electrophoresis. In the 3H ODC trial 4 different pCO2 levels and 4 different temperatures will be analyzed in the resulting 16 combinations. In each round a lot of ODCs will be measured, the measurement chamber will be filled with participants blood samples in a randomized manner. After the measurements, the blood samples will be discarded.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoxia, Hypothermia, Accidental, Hypercapnia, Avalanche, Landslide, or Mudslide
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
16 combinations of 4 levels of pCO2 and 4 levels of temperature will be assessed for each participant
Masking
Investigator
Allocation
N/A
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Other
Intervention Name(s)
blood sampling
Intervention Description
venous blood sampling for oxygen affinity in-vitro test
Primary Outcome Measure Information:
Title
amount of p50 in different levels of hypercapnia and hypothermia
Description
amount of p50 in mmHg (p50 = pO2 when oxygen saturation of hemoglobin is 50%)
Time Frame
day 1
Secondary Outcome Measure Information:
Title
amount of p50 shift due to sex
Description
amount of p50 in mmHg (p50 = pO2 when oxygen saturation of hemoglobin is 50%)
Time Frame
day 1
Title
amount of inflection point in different levels of hypercapnia and hypothermia
Description
amount of inflection point in mmHg
Time Frame
day 1
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18-40 years
fasted situation
ASA I
Informed Consent
Exclusion Criteria:
any drug abuse
any drug intake within the last 10 days
smoking
known hemoglobinopathy
relevant illness within last 14 days
relevant blood loss within last 14 days
pregnancy or breast-feeding
participation in any pharmacological study
exposure to high altitude (> 3000 m) within last 4 weeks
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mathias Ströhle, MD
Organizational Affiliation
Medical University Innsbruck
Official's Role
Principal Investigator
Facility Information:
Facility Name
General and Surgical Critical Care Medicine, Medical University of Innsbruck
City
Innsbruck
ZIP/Postal Code
6020
Country
Austria
12. IPD Sharing Statement
Plan to Share IPD
No
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Triple H ODC Trial
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