Status:

UNKNOWN

HA Residents With PVD, Pulmonary Artery Pressure (PAP) Assessed at HA (2840m) With and Without Supplemental Oxygen Therapy (SOT)

Lead Sponsor:

University of Zurich

Conditions:

Pulmonary Vascular Disorder

Pulmonary Artery Hypertension

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

To study the effect of SOT in patients with pulmonary vascular diseases (PVD) defined as pulmonary arterial hypertension or chronic thromboembolic pulmonary hypertension (PH) who permanently live \>25...

Detailed Description

Patients with PVD diagnosed with precapillary PH with right heart catheterization and classified to groups 1 and 4 (PAH or CTEPH) who permanently live at HA \>2500 (PVDHA) will have echocardiografy to...

Eligibility Criteria

Inclusion

  • Adult patients 18-80 years old of both genders,
  • Residence \> 2500m of altitude
  • diagnosed with precapillary PH (mean pulmonary artery pressure (mPAP) \>20 mmHg, pulmonary artery wedge pressure (PAWP) ≤15 mmHg and pulmonary vascular resistance (PVR) ≥2 wood units (WU) by right heart catheterization) with PH being classified as PAH or CTEPH according to guidelines
  • Patients stable on therapy
  • New York Heart Association (NYHA) functional class I-III
  • Provided written informed consent to participate in the study.

Exclusion

  • Age \<18 years or \>80 years
  • unstable condition
  • Patients who cannot follow the study investigations, patient permanently living \< 2500m.
  • 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 have persistent oxygen saturation by pulseoximetry (SpO2) \<80% on ambient air.
  • Patients with chronic mountain sickness (Hemoglobin \> 19 g/dl in women, \>21 g/dl in men)
  • Patient with a non-corrected ventricular septum defect
  • Relevant concomitant other disease of the heart, kidney, liver, blood (anemia hemoglobin\<11 g/dl)

Key Trial Info

Start Date :

July 5 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2023

Estimated Enrollment :

24 Patients enrolled

Trial Details

Trial ID

NCT06084559

Start Date

July 5 2023

End Date

December 31 2023

Last Update

October 16 2023

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University Hospital Zürich

Zurich, Switzerland, 8091