Acute Exposure of High Altitude on Cognitive Function

Pulmonary Hypertension Clinical Trial

Official title:

Acute Exposure to Hypoxia in Precapillary Pulmonary Hypertension: Physiological and Clinical Effects at Rest and During Exercise

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03637192
• Other study ID #: 2018-00455_B6
• Status: Completed
• Phase: N/A
• Start date: July 1, 2018
• Est. completion date: January 1, 2019

Study information

• Verified date: January 2020
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Randomized crossover Trial in patients with pulmonary arterial hypertension (PAH) or chronic thromboembolic pulmonary Hypertension (CTEPH) to assess the acute response to High Altitude (2500m above sea level) on cognitive functions

Description:

Low altitude baseline measurements will be performed in Zurich (460m) including Echocardiography, Right heart catheterization, 6 Minute walk test, pulmonary function test, clinical assessment and blood gas analysis.

Randomly assigned to the order of testing, the participants will be tested in Low Altitude (Zurich, 470m) and at High Altitude (2500m).

During the exposure to High Altitude (Säntis; 2500m above sea level) for approximately 5 hour, the participants will perform cognitive function test .

The results will be compared to low altitude in Zurich (470m).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: January 1, 2019
• Est. primary completion date: January 1, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Informed consent

• PH diagnosed according to internation Guidelines: mPAP = 25 mmHg along with a PAWP =15 mmHg during right heart catheterization at the time of Initial diagnosis

• PH class 1 (PAH) or 4 (CTEPH)

• Stable condition, on the same medication for > 4 weeks

• Patient live permanently at an altitude < 1000m asl.

Exclusion Criteria:

• Resting PaO2 =7.3 kPA corresponding to the requirement of long-term oxygen therapy > 16hour daily (nocturnal oxygen therapy alone is allowed)

• Severe daytime hypercapnia (pCO2 > 6.5 kPa)

• Susceptibility to high altitude related diseases (AMS, HAPE, etc.) based on previous experienced discomfort at altitudes.

• Exposure to an altitude >1500m for =3 nights during the last 4 weeks before the study participation

• Residence > 1000m above sea level

• Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, neurological or orthopedic problems with Walking disability

• Women who are pregnant or breast feeding

Related Conditions & MeSH terms

• Hypertension
• Hypertension, Pulmonary
• Pulmonary Hypertension

Intervention

Other:
• Low altitude: 470m above sea level
Assessment at Low Altitude (in Zurich; 470m above sea level) in order to compare this data with High altitude exposure
• Säntis; 2500m above sea Level
Exposure to High Altitude (Säntis; 2500m above sea level) for approximately 5 hours

Locations

Country	Name	City	State
Switzerland	Respiratory Clinic, University Hospital of Zurich	Zurich

Sponsors (1)

Lead Sponsor	Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cognitive Function test	Change in cognitive function test time during the exposure to High altitude (Säntis ; 2500m above sea level) compared to low altitude (Zurich)	1 day at altitude