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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

Key facts

Where
Zurich, SwitzerlandSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07804693, who can take part

Where in Switzerland

  • University Hospital of ZurichZurich, SwitzerlandNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Silvia Ulrich Somaini
Trial code
NCT07804693
Record updated
4 September 2026
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: 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.

Exclusion: Patients with moderate to severe concomitant lung disease (FEV1<70% or forced vital capacity <70%), severe parenchymal lung disease, severe smokers (>20 cigarettes/day); unstable condition; Relevant concomitant other disease of the heart, kidney, liver, blood (anemia hemoglobin<11 g/dl); Age <18 years or >80 years; 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; 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.

ClinicalTrials.gov NCT07804693