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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06092424
Other study ID # PVD_HAvsLA_PAP
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date September 23, 2023
Est. completion date December 31, 2024

Study information

Verified date October 2023
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To study the effect of relocation from 2840m (Quito) to sea level (Pedernales) in patients with pulmonary vascular diseases (PVD) defined as pulmonary arterial hypertension or chronic thromboembolic pulmonary hypertension (PH) who permanently live >2500m on pulmonary artery pressure (PAP) and other hemodynamics.


Description:

This research in 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 (PVD_HA) will have PAP and other hemodynamics assessed by echocardiography and blood gases near their living altitude in Quito at 2840m and at sea level in Pedernales the day after the first and the second night after relocation.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 36
Est. completion date December 31, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Adult patients 18-90 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 Criteria: - 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 pulse-oximetry (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)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Relocation from HA to LA
Patients will be relocated by bus from Quito (2840m) to Pedernales (sea level) and have investigations at both altitudes

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 Pulmonary artery Pressure (PAP) in the morning of second day at sea level (LA) Change in PAP in mmHg assessed by echocardiography between LA (sea level) vs High altitude (HA) in the morning of the second day at sea level
Secondary Cardiac output in the morning of the second day at sea level Change in cardiac output in l/min assessed by echocardiography between LA (sea level) vs HA (2840 m) in the morning of the second day at sea level
Secondary Cardiac output in the morning of the third day at sea level Change in cardiac output in l/min assessed by echocardiography between LA (sea level) vs HA (2840m) in the morning of the third day at sea level
Secondary Tricuspid pressure gradient by echocardiography in the morning of the second day at sea level Tricuspid pressure gradient assessed by echocardiography between LA (sea level) vs HA (2840m) in the morning of the second day at sea level
Secondary Tricuspid pressure gradient by echocardiography in the morning of the third day at sea level Tricuspid pressure gradient assessed by echocardiography assessed by between LA (sea level) vs HA (2840m) in the morning of the third day at sea level
Secondary Tricupsid annular plane systolic excursion by echocardiography in the morning of the second day at sea level Tricupsid annular plane systolic excursion assessed by echocardiography assessed by between LA (sea level) vs HA (2840m) in the morning of the third day at sea level
Secondary Tricupsid annular plane systolic excursion by echocardiography in the morning of the third day at sea level Tricupsid annular plane systolic excursion by echocardiography assessed by between LA (sea level) vs HA (2840m) in the morning of the third day at sea level
Secondary ph by arterial blood gases in the morning of the second day at sea level Change in ph by arterial blood gases assessed between LA (sea level) vs HA (2840m) in the morning of the second day at sea level
Secondary partial pressure of oxygen (PaO2) by arterial blood gases in the morning of the second day at sea level Change in partial pressure of oxygen (PaO2) assessed by arterial blood gases between LA (sea level) vs HA (2840m) in the morning of the second day at sea level
Secondary partial pressure of carbon dioxide (PaCO2) by arterial blood gases in the morning of the second day at sea level Change in partial pressure of carbon dioxide (PaCO2) assessed by arterial blood gases partial pressure of carbon dioxide (PaCO2) between LA (sea level) vs HA (2840m) in the morning of the second day at sea level
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