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NCT06489704Completed

High Altitude (HA) Residents With High Altitude Pulmonary Hypertension (HAPH), Pulmonary Artery Pressure (PAP) Assessed at HA (3200 m) vs LA (760 m)

Comparative Study of Pulmonary Artery Pressure (PAP) Assessed by Echocardiography in Patients With High Altitude Pulmonary Hypertension (HAPH) Permanently Residing Above 2500 Meters When Assessed Near Resident High Altitude (HA) at 3200 m vs. at Low Altitude (LA) at 760 m

Source: ClinicalTrials.gov · Last updated 21 Jan 2026

Brief summary (registry, in English)

To study the effect of relocation from 3200 m (Aksay) to 760 m (Bishkek) in patients with high altitude pulmonary hypertension (HAPH) who permanently live \>2500 m on pulmonary artery pressure (PAP)

Status (registry)
Completed
Study type
Interventional
Enrollment
24 (actual)
First submitted
28 Jun 2024
Start date
2 Jul 2024
Primary completion date
27 Sept 2024
Lead sponsor
University of Zurich
NCT number
NCT06489704

What you commit to

  • Study type: Interventional
  • Participants enrolled: 24
  • From 2 Jul 2024 to the primary completion date, 27 Sept 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with moderate to severe concomitant lung disease (FEV1\<70% or forced vital capacity \<70%), severe parenchymal lung disease, heavy smoking \>20 cigarettes/day or \>20 pack-years.
  • Regular use of medication that affects control of breathing (benzodiazepines, opioids, acetazolamide)

Other illness

  • Coexistent unstable systemic hypertension or coronary artery disease that required adjustment of medication within the last 2 months

Other

  • Highlanders who cannot follow the study investigations,

Who the study is looking for

  • Permanently living \>2500 m
  • HAPH diagnosed with a minimum RV/RA of 30 mmHg assessed by echocardiography at an altitude of 3200 m
  • Written informed consent

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Aksay Medical Center
Coordinator of this site? Confirm its status
Aksay Plateau, Naryn, Kyrgyzstan, KyrgyzstanKyrgyzstanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.