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HA Residents With PVD, 6MWD Assessed at HA (2840m) vs LA (Sea Level)

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Active, not recruiting

Conditions

Pulmonary Artery Hypertension
Chronic Thromboembolic Pulmonary Hypertension
Pulmonary Vascular Disease

Treatments

Behavioral: Relocation to sea level

Study type

Interventional

Funder types

Other

Identifiers

NCT05996302
PVD_HAvsLA_6MWD

Details and patient eligibility

About

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 6-minute walk distance (6MWD)

Full 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 (PVDHA) will have 6-minute walk distance 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.

Enrollment

24 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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 WU (wood units) by right heart catheterization) with PH being classified as PAH or CTEPH according to guidelines
  • Patients stable on therapy
  • NYHA (new york heart association) 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 igarettes/day)
  • Severely hypoxemic patients at Quito permanently have persistent SpO2 (oxygen saturation by pulseoximetry) <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)

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

24 participants in 2 patient groups

6-minute walk distance at 2840m
Active Comparator group
Description:
Participants will have 6-minute walk distance (6MWD) assessment near their resident altitude at 2840m
Treatment:
Behavioral: Relocation to sea level
6-minute walk distance at sea level
Experimental group
Description:
Participants will have 6-minute walk distance (6MWD) assessment at sea level (0-30m)
Treatment:
Behavioral: Relocation to sea level

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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