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

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

High Altitude Pulmonary Hypertension

Treatments

Other: SDB assessment

Study type

Interventional

Funder types

Other

Identifiers

NCT06489717
HAPH_HAvsLA_SDB

Details and patient eligibility

About

To study the effect of relocation from 3200m (Aksay) to 760m (Bishkek) in highlanders with High Altitude Pulmonary Hypertension (HAPH) who permanently live >2500m on sleep disordered breathing

Full description

This research in highlanders with HAPH diagnosed by echocardiography and defined by a RV/RA >30 mmHg who permanently live at HA >2500 m will have nocturnal respiratory sleep studies near their living altitude in Aksay at 3200 m and on night 1 and 6 at 760m after relocation.

Enrollment

24 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • Highlanders who cannot follow the study investigations,
  • 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.
  • Coexistent unstable systemic hypertension or coronary artery disease that required adjustment of medication within the last 2 months
  • Regular use of medication that affects control of breathing (benzodiazepines, opioids, acetazolamide)

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 1 patient group

Assessments at 3200 m and 760 m, respectively
Experimental group
Description:
Participants will have a SDB assessment near their resident altitude at 3200 m and after relocation to 760 m after 1 and 7 days
Treatment:
Other: SDB assessment

Trial contacts and locations

1

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Central trial contact

Michael Furian, Prof. Dr.; Silvia Ulrich, Prof. Dr.

Data sourced from clinicaltrials.gov

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