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Effect of Bosentan on Exercise Capacity at High Altitude

Effect of Bosentan on Exercise Capacity at High Altitude

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00432978
Enrollment
20
Registered
2007-02-08
Start date
2006-07-31
Completion date
2007-02-28
Last updated
2007-04-18

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

Conditions

Altitude, Pulmonary Hypertension

Keywords

hypoxia, endothelin, exercise

Brief summary

This study is to determine whether bosentan will alter exercise capacity after rapid ascent to high altitude. We hypothesize that bosentan administration will improve arterial oxygenation and exercise capacity.

Detailed description

Both the prostacyclin and the nitric oxide pathways are important in modulating hypoxic pulmonary vasoconstriction (HPV). There is little information about the role of the endothelin pathway at high altitude. The endothelin pathway involves the activation of two distinct receptors, A and B. Bosentan is a nonpeptide, specific, competitive, dual antagonist of both endothelin receptor subtypes. The primary objective of this study will be to determine the effect of endothelin receptor blockade with bosentan on exercise performance and HPV. This is a prospective, double blind, placebo-controlled, randomized cross-over study involving healthy subjects aged 25-55 years of age. Subjects will undergo echocardiography and exercise testing at low altitude (\< 500m) and at 3800m. Subjects will receive either bosentan vs. placebo and will be studied at low and high altitude on two occasions in a crossover design. Primary outcome measures will be pulmonary artery systolic pressure measured by echo-Doppler and exercise capacity. A better understanding of the role of the endothelin pathway in HPV may lead to improved treatments for some patients.

Interventions

Sponsors

Actelion
CollaboratorINDUSTRY
VA Loma Linda Health Care System
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Normal healthy subjects aged 18 - 55 years

Exclusion criteria

* Pregnancy * Heart, lung or liver disease * Use of glyburide, cyclosporin A

Design outcomes

Primary

MeasureTime frame
Exercise Capacity
Pulmonary artery systolic pressure

Secondary

MeasureTime frame
Hemoglobin oxygen saturation

Countries

United States

Outcome results

None listed

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