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CompletedNCT01875133Updated May 19, 2015

Patients With Chronic Obstructive Pulmonary Disease At Altitude

An interventional study of altitude exposure in Chronic Obstructive Pulmonary Disease (COPD), sponsored by University of Zurich. Completed at 1 site in Switzerland. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2015-05-19.

Sponsored by University of Zurich · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

The purpose of this study is to investigate the effect of a stay at moderate altitude on exercise performance of patients with chronic obstructive lung disease.

Read the detailed description

Patients with moderate to severe COPD living below 800 m, will be recruited to participate in a randomized cross-over field trial evaluating the hypothesis that exercise capacity during a 4 day sojourn at moderate altitude is reduced in comparison to low altitude. Outcomes will be assessed during 2 days in Zurich (490 m, low altitude baseline), 2 days at Davos Clavadel (1650 m), and 2 days at Davos Jakobshorn (2590 m). The main outcome is the 6 minute walk distance.

02

Conditions studied

  • Chronic Obstructive Pulmonary Disease (COPD)

Keywords

  • airway disease
  • bronchitis
  • emphysema
  • lung
03

In context

Pulmonary Disease, Chronic Obstructive

4,252 studies on the registry are indexed under Pulmonary Disease, Chronic Obstructive; 707 are open to participants now.

This study's planned enrollment of 50 is below the median of 70 across 3,008 interventional studies indexed under Pulmonary Disease, Chronic Obstructive.

Browse Pulmonary Disease, Chronic Obstructive studies →

Lead sponsor

University of Zurich is the lead sponsor of 1,048 studies on the registry; 131 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • chronic obstructive pulmonary disease (COPD), GOLD grade 2-3
  • residents at low altitude (\<800 m)

Exclusion criteria

Exclusion Criteria:

  • Unstable condition, COPD exacerbation
  • Mild (GOLD 1) or very severe COPD (GOLD 4)
  • requirement for oxygen therapy at low altitude residence
  • hypoventilation
  • pulmonary hypertension
  • more than mild or unstable cardiovascular disease
  • use of drugs that affect respiratory center drive
  • internal, neurologic or psychiatric disease that interfere with protocol compliance including current heavy smoking (>20 cigarettes per day), inability to perform 6 min walk test.
  • previous intolerance to moderate altitude (\<2600m).
  • Exposure to altitudes >1500m for >2 days within the last 4 weeks before the study.
  • Pregnant or nursing patients
05

Study design

Phase
Not applicable
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Other
    A: low-intermediate-high altitude

    Altitude exposure sequence A, 490-1630-2590m

    Other: altitude exposure

  • Other
    B: low-high-intermediate altitude

    Altitude exposure sequence B, 490-2590-1630 m

    Other: altitude exposure

  • Other
    C: intermediate-high-low altitude

    Altitude exposure sequence C, 1630-2590-490 m

    Other: altitude exposure

  • Other
    D: high-intermediate-low altitude

    Altitude exposure sequence D, 2590-1630-490 m

    Other: altitude exposure

Interventions

  • Otheraltitude exposure

    stay at different altitudes: 490, 1630, 2590 m

06

What researchers measure

Primary outcomes

  1. Change in exercise performance from baseline measured at 490 m

    6 min walk distance

    Time frame: Change in 6 min walk distance from 490 m baseline during 2 days at 2590 m

Secondary outcomes

  1. Change in exercise performance from baseline measured at 490 m

    6 min walk distance

    Time frame: Change in 6 min walk distance from 490 m baseline during 2 days at 1650 m

  2. Change in pulmonary function from baseline measured at 490 m

    lung volumes by spirometry

    Time frame: Change in pulmonary function from 490 m baseline during 2 days at 2590 m

  3. Change in pulmonary function from baseline measured at 490 m

    lung volumes by spirometry

    Time frame: Change in pulmonary function from 490 m baseline during 2 days at 1650 m

  4. Change in arterial blood gases from baseline measured at 490 m

    Arterial blood gas analysis

    Time frame: Change in arterial blood gases from 490 m baseline during 2 days at 2590 m

  5. Change in arterial blood gases from baseline measured at 490 m

    Arterial blood gas analysis

    Time frame: Change in arterial blood gases from 490 m baseline during 2 days at 1650 m

  6. Change in perceived exertion from baseline measured at 490 m

    Borg CR10 scale at end of 6 min walk

    Time frame: Change in perceived exertion from 490 m baseline during 2 days at 2590 m

  7. Change in perceived exertion from baseline measured at 490 m

    Borg CR10 scale at end of 6 min walk

    Time frame: Change in perceived exertion from 490 m baseline during 2 days at 1650 m

07

Study locations

1 site
  • University Hospital Zurich, Pulmonary Division
    Zurich, CH-8091, Switzerland
08

References and documents

Publications

  • Schwarz EI, Latshang TD, Furian M, Fluck D, Segitz S, Muller-Mottet S, Ulrich S, Bloch KE, Kohler M. Blood pressure response to exposure to moderate altitude in patients with COPD. Int J Chron Obstruct Pulmon Dis. 2019 Mar 14;14:659-666. doi: 10.2147/COPD.S194426. eCollection 2019. PubMed 30936690 ↗
  • Furian M, Flueck D, Latshang TD, Scheiwiller PM, Segitz SD, Mueller-Mottet S, Murer C, Steiner A, Ulrich S, Rothe T, Kohler M, Bloch KE. Exercise performance and symptoms in lowlanders with COPD ascending to moderate altitude: randomized trial. Int J Chron Obstruct Pulmon Dis. 2018 Oct 26;13:3529-3538. doi: 10.2147/COPD.S173039. eCollection 2018. PubMed 30464436 ↗
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Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of May 2013, a primary completion of Dec 2013 and a completion of Dec 2013. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
May 29, 2013
First posted
Jun 11, 2013
Start
May 2013
Primary completionActual
Dec 2013
CompletionActual
Dec 2013
Last update
May 19, 2015
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 19, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01875133
Responsible party
Sponsor
First posted
Jun 11, 2013
Start date
May 2013
Primary completion
Dec 2013
Completion
Dec 2013
Last update
May 19, 2015

Study contacts

Konrad E Bloch, MD
study chair · University Hospital, Zürich
Tsogyal D Latshang, MD
principal investigator · University Hospital, Zürich

Oversight

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

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This study is completed, as verified in May 2015. You cannot join it, but the record below documents what was studied.

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