Assessment of Total Pulmonary Resistance sPAP/CO Between Sea Level LA vs. High Altitude HA After Re-ascent in Patients With Pulmonary Arterial Hypertension PAH
Effect of a One-week Descent From 2850m to Sea Level and Re-ascent in Patients With Pulmonary Arterial Hypertension and Healthy Controls Permanently Living > 2600m on Pulmonary Hemodynamics, Exercise Capacity, Blood Oxygenation, Sleep Disordered Breathing and Further Outcomes
1 other identifier
interventional
20
1 country
1
Brief Summary
To study the effect of a re-ascent after a one-week stay at sea level (after prior descent from 2850m) to high altitude (Quito Ecuador: 2850m) on pulmonary resistance (sPAP/CO) and other hemodynamic outcomes in patients with pulmonary arterial hypertension PAH, who live permanently \>2600m.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 17, 2026
CompletedFirst Posted
Study publicly available on registry
September 4, 2026
CompletedStudy Start
First participant enrolled
September 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 4, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
ExpectedSeptember 4, 2026
August 1, 2026
9 days
August 17, 2026
August 31, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pulmonary resistance (sPAP/CO) after re-ascent to 2850m
Difference in sPAP/CO by echocardiography between sea level (after one-week stay) and day after re-ascent at 2850m in patients with pulmonary arterial hypertension
From Day 5-7 at sea level to day after re-ascent
Secondary Outcomes (21)
Tricuspid regurgitation velocity TRV after re-ascent to 2850m
From Day 5-7 at sea level to day after re-ascent
Cardiac output CO after re-ascent to 2850m
From Day 5-7 at sea level to the day after re-ascent
Tricuspid annular plan systolic excursion TAPSE after re-ascent to 2850m
From Day 5-7 at sea level to day after re-ascent
Right ventricular strain after re-ascent to 2850m
From Day 5-7 at sea level to day after re-ascent
Right atrial pressure RAP after re-ascent to 2850m
From Day 5-7 at sea level to day after re-ascent
- +16 more secondary outcomes
Study Arms (1)
Pulmonary resistance (sPAP/CO) at sea level and after re-ascent at 2850m
EXPERIMENTALAssessment of pulmonary resistance (sPAP/CO) and other hemodynamic parameters after 7 days at sea level with re-ascent from sea level back to 2850m by bus (in one day) and assessment of the same outcomes
Interventions
After 7 days at sea level return/re-ascent to their usual living altitude at 2850m
Eligibility Criteria
You may qualify if:
- Adult patients aged 18-80 years and of all genders
- Permanent residence \> 2600 m
- Diagnosis of pulmonary arterial hypertension PAH (PAHHA-Group) according to guidelines
- Patients are stable on therapy
- NYHA (new york heart association) functional class I-III.
- written informed consent to participate in the study.
You may not qualify if:
- Age \<18 years or \>80 years
- unstable condition
- Patients who cannot follow the study investigations
- Patient permanently living \< 2600m.
- Patients who traveled and stayed overnight at altitudes \<2000 m in the past 4 weeks.
- Patients with moderate to severe concomitant lung disease (FEV1\<70% or forced vital capacity \<70%), severe parenchymal lung disease, severe smokers (\>20 cigarettes/day)
- Severely hypoxemic patients at Quito permanently having persistent SpO2 (oxygen saturation by pulseoximetry) \<80% on ambient air.
- Patient with a non-corrected ventricular septum defect
- Relevant concomitant other disease of the heart, kidney, liver, blood (anemia hemoglobin\<11 g/dl)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital of Zurich
Zurich, 8091, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Silvia Ulrich
University Hospital Zurich, Departement of Pulmonology
- PRINCIPAL INVESTIGATOR
Rodrigo Hoyos
Hospital Carlos Andrade Marin of Quito, Ecuador
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Prof. Dr. med.
Study Record Dates
First Submitted
August 17, 2026
First Posted
September 4, 2026
Study Start
September 25, 2026
Primary Completion
October 4, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
September 4, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will share
Data will be provided upon request and based on a clear intention reviewed by an ethical review board