Trials / Completed
CompletedNCT03637127
Acute Exposure of Simulated Hypoxia on Cognitive Function
Acute Exposure to Hypoxia in Precapillary Pulmonary Hypertension: Physiological and Clinical Effects at Rest and During Exercise
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 28 (actual)
- Sponsor
- University of Zurich · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Randomized crossover Trial in patients with Pulmonary Hypertension (PAH, CTEPH) to assess the acute response to simulated altitude (FiO2:15.1, equivalent to 2500m above sea level) on cognitive functions.
Detailed description
Low altitude baseline measurements will be performed in Zurich (460m asl) including Echocardiography, Right heart catheterization, six-minute walk test (6MWT), pulmonary function test, clinical assessment and blood gas Analysis. Randomly assigned to the order of testing, the participants will be tested under simulated altitude (FiO2: 15.1% with the "AMC Altitrainer") and shamed altitude with the same device. During the exposure to simulated altitude (FiO2: 15.1%) of approximately 1 hour, the participants will perform cognitive function test . The results will be compared under hypoxic and normal conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Simulated Altitude (FiO2: 15.1%) | Inhalation of deoxygenated air through a altitude simulator ("Altitrainer"), for approx. 1 hour. given by a facemask. |
| DEVICE | Shamed Hypoxia (FiO2: 20.9) | Inhalation of unmodified air through an altitude Simulator ("Altitrainer") for approximately 1 hour given by a facemask |
Timeline
- Start date
- 2018-07-01
- Primary completion
- 2019-04-01
- Completion
- 2019-04-01
- First posted
- 2018-08-17
- Last updated
- 2020-01-07
Locations
1 site across 1 country: Switzerland
Source: ClinicalTrials.gov record NCT03637127. Inclusion in this directory is not an endorsement.