ClinicalTrials.Veeva

Menu

Patients With Chronic Obstructive Pulmonary Disease At Altitude

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Chronic Obstructive Pulmonary Disease (COPD)

Treatments

Other: altitude exposure

Study type

Interventional

Funder types

Other

Identifiers

NCT01875133
2013-0088

Details and patient eligibility

About

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.

Full 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.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

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

Trial design

50 participants in 4 patient groups

A: low-intermediate-high altitude
Other group
Description:
Altitude exposure sequence A, 490-1630-2590m
Treatment:
Other: altitude exposure
B: low-high-intermediate altitude
Other group
Description:
Altitude exposure sequence B, 490-2590-1630 m
Treatment:
Other: altitude exposure
C: intermediate-high-low altitude
Other group
Description:
Altitude exposure sequence C, 1630-2590-490 m
Treatment:
Other: altitude exposure
D: high-intermediate-low altitude
Other group
Description:
Altitude exposure sequence D, 2590-1630-490 m
Treatment:
Other: altitude exposure

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems