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CompletedNCT00514826Updated May 26, 2010

Study to Investigate Sleep Apnea Patients at Altitude

An interventional study of altitude exposure in Obstructive Sleep Apnea Syndrome, sponsored by University of Zurich. Completed at 1 site in Switzerland. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2010-05-26.

Sponsored by University of Zurich · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
20 Years and older
Sex
All
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Study summary

The purpose of the study is to investigate the effect of an altitude sojourn on patients with the obstructive sleep apnea syndrome

Read the detailed description

Previous observations do not allow to draw firm conclusions on the effect of altitude sojourn on sleep, breathing and daytime performance in patients with the obstructive sleep apnea syndrome. Furthermore, the susceptibility of sleep apnea patients to high altitude related illness is not known. Therefore, the purpose is to study untreated patients with obstructive sleep apnea syndrome living at low altitude during a sojourn of a few days at moderate altitude in order to evaluate the physiologic effects of hypobaric hypoxia in these patients. We hypothesize that: 1. Sleep and nocturnal breathing disturbances in untreated OSA patients are more pronounced at moderate altitude compared to low altitude. 2. The increase in sleep related breathing disturbances at moderate altitude is due to an increase in central apnea/hypopnea

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Conditions studied

  • Obstructive Sleep Apnea Syndrome
03

In context

Apnea

1,423 studies on the registry are indexed under Apnea; 160 are open to participants now.

This study's planned enrollment of 40 is below the median of 51 across 966 interventional studies indexed under Apnea.

Browse Apnea studies →

Lead sponsor

University of Zurich is the lead sponsor of 1,030 studies on the registry; 130 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Obstructive sleep apnea syndrome based on symptoms and a sleep study

Exclusion criteria

Exclusion Criteria:

  • Sleep disorders other than obstructive sleep apnea syndrome
  • Other than mild, stable cardiovascular disease
  • Other than mild lung disease
  • Chronic rhinitis, previous uvulopalatopharyngoplasty
  • Treatment with drugs that affect respiratory center drive
  • Internal, neurologic or psychiatric disease that interferes with sleep quality
  • Previous intolerance to moderate or low altitude \< 2600m
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Study design

Phase
Not applicable
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Interventions

  • Otheraltitude exposure

    sojourn at moderate altitude (1860m and 2590m) during 2 days/nights each

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What researchers measure

Primary outcomes

  1. Prevalence and severity of sleep disordered breathing

    Time frame: during altitude sojourn

Secondary outcomes

  1. alterations in sleep structure and vigilance; high altitude related illness

    Time frame: during altitude sojourn

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Study locations

1 site
  • Pulmonary Division, University Hospital Zurich, Switzerland
    Zurich, CH-8091, Switzerland
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References and documents

Publications

  • Nussbaumer-Ochsner Y, Schuepfer N, Ulrich S, Bloch KE. Exacerbation of sleep apnoea by frequent central events in patients with the obstructive sleep apnoea syndrome at altitude: a randomised trial. Thorax. 2010 May;65(5):429-35. doi: 10.1136/thx.2009.125849. PubMed 20435865 ↗
  • Bloch KE, Latshang TD, Turk AJ, Hess T, Hefti U, Merz TM, Bosch MM, Barthelmes D, Hefti JP, Maggiorini M, Schoch OD. Nocturnal periodic breathing during acclimatization at very high altitude at Mount Muztagh Ata (7,546 m). Am J Respir Crit Care Med. 2010 Aug 15;182(4):562-8. doi: 10.1164/rccm.200911-1694OC. Epub 2010 May 4. PubMed 20442435 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 26, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00514826
Lead sponsor
University of Zurich
First posted
Aug 10, 2007
Start date
Aug 2007
Primary completion
Oct 2007
Completion
Oct 2007
Last update
May 26, 2010

Study contacts

Konrad E. Bloch, MD
study director · Pulmonary Division, University Hospital Zurich, Switzerland

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2010. You cannot join it, but the record below documents what was studied.

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