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

Comparative Study of Sleep Disordered Breathing (SDB) in Patients With High Altitude Pulmonary Hypertension Permanently Residing Above 2500 Meters When Assessed Near Resident High Altitude (HA) at 3200 m vs. at Low Altitude (LA) 760 m

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06489717
Enrollment
24
Registered
2024-07-08
Start date
2024-07-02
Completion date
2024-07-12
Last updated
2026-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Altitude Pulmonary Hypertension

Keywords

Pulmonary Hypertension, Hypoxia, High Altitude, Sleep disordered breathing

Brief summary

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

Detailed 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.

Interventions

OTHERSDB assessment

SDB will be assessed by respiratory polygraphy according to clinical standards

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Each highlander with HAPH will be assessed for SDB at 3200 m and at 760 m according to a prospective study design

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Mean nocturnal SpO2 during the first night at LA vs HAnight 1 at 760 m compared to 3200 m.Change in mean nocturnal SpO2 (%) between LA (760 m) vs HA (3200 m)

Secondary

MeasureTime frameDescription
Mean nocturnal SpO2 during the sixth night at LA vs HAnight 6 at 760 m compared to 3200 m.Change in mean nocturnal SpO2 (%) between LA (760 m) vs HA (3200 m)
Time spent with SpO2<90% at LA vs HAnight 1 and night 6 at 760 m compared to 3200 m.Change in time spent with SpO2\<90% between LA (760 m) vs HA (3200 m)
AHI at LA vs HAnight 1 and night 6 at 760 m compared to 3200 m.Change in apnea-hypopnea index (AHI) between LA (760 m) vs HA (3200 m)
ODI at LA vs. HAnight 1 and night 6 at 760 m compared to 3200 m.Change in oxygen desaturation index (ODI) between LA (760 m) vs HA (3200 m)
Time spent with periodic breathing at LA vs. HAnight 1 and night 6 at 760 m compared to 3200 m.Change in time spent with periodic breathingbetween LA (760 m) vs HA (3200 m)
Heart rate variability at LA vs. HAnight 1 and night 6 at 760 m compared to 3200 m.Change in heart rate variability between LA (760 m) vs HA (3200 m)
ECG markers of repolarization at LA vs. HAnight 1 and night 6 at 760 m compared to 3200 m.Change in electrocardiogram (ECG) markers of repolarization (QT time) between LA (760 m) vs HA (3200 m)
pulse transit time drops at LA vs. HAnight 1 and night 6 at 760 m compared to 3200 m.Change in pulse transit time drops between LA (760 m) vs HA (3200 m)

Countries

Kyrgyzstan

Contacts

PRINCIPAL_INVESTIGATORTalant M Sooronbaev, Prof. Dr.

National Center of Cardiology and Internal Medicine named after academician M.Mirrakhimov

PRINCIPAL_INVESTIGATORSilvia Ulrich, Prof. Dr.

University Hospital Zurich, Department of Pulmonology

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026