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Effects of Iloprost on Hypoxic Pulmonary Vasoconstriction and Exercise Capacity at High Altitude

Primary Purpose

Hypoxic Pulmonary Vasoconstriction

Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
iloprost
Sponsored by
VA Loma Linda Health Care System
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional basic science trial for Hypoxic Pulmonary Vasoconstriction focused on measuring To study the effects of iloprost on hypoxic pulmonary vasoconstriction at high altitude

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age: 18 - 80 years
  2. Healthy physically active males or females
  3. Have readily measurable tricuspid regurgitation (TR) peak systolic velocity by continuous wave Doppler ultrasound

Exclusion Criteria:

  1. Unable to measure TR velocity
  2. Known liver disease
  3. Pregnancy
  4. Nitrates, cyclosporin, glyburide or other medications that in the opinion of the investigators could place subjects at increased risk of complications
  5. Any other medical condition that in the opinion of the investigators would place the subject at high risk

Sites / Locations

  • Jerry L. Pettis VA Medical CenterRecruiting

Outcomes

Primary Outcome Measures

Exercise capacity, pulmonary artery systolic pressure, cardiac output, oxygen saturation

Secondary Outcome Measures

Heart rate, tissue Doppler echocardiographic measurements

Full Information

First Posted
June 30, 2008
Last Updated
July 1, 2008
Sponsor
VA Loma Linda Health Care System
Collaborators
Actelion
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1. Study Identification

Unique Protocol Identification Number
NCT00708565
Brief Title
Effects of Iloprost on Hypoxic Pulmonary Vasoconstriction and Exercise Capacity at High Altitude
Official Title
Effects of Iloprost on Hypoxic Pulmonary Vasoconstriction and Exercise Capacity at High Altitude
Study Type
Interventional

2. Study Status

Record Verification Date
June 2008
Overall Recruitment Status
Unknown status
Study Start Date
July 2008 (undefined)
Primary Completion Date
October 2008 (Anticipated)
Study Completion Date
October 2008 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
VA Loma Linda Health Care System
Collaborators
Actelion

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to determine if single dose administration of inhaled iloprost will reduce pulmonary artery pressure, reduce hypoxic pulmonary vasoconstriction and improve arterial oxygenation at rest and during exercise at high altitude.
Detailed Description
Three major pathways in addition to oxygen modulate pulmonary vascular tone: 1) nitric oxide, 2) endothelin, and 3) prostacyclin. Considerable animal data support the role of the prostacyclin pathway in modulating hypoxic pulmonary vasoconstriction. In humans, prostacyclin and its analogs are important therapeutic agents in the treatment of pulmonary arterial hypertension (PAH). Despite the animal data and human data in PAH there is very little information about the use of iloprost to relieve hypoxic pulmonary vasoconstriction in healthy humans. Inhaled iloprost is an ideal agent to study the prostacyclin pathway due to its short duration of action (30-90 min) and elimination half-life of only 20-30 min. Individuals already participating in the Nepal Medex 2008 trip will be invited to participate in this research. Participants will be healthy active females or males, between 18-80 years of age, without known pregnancy or liver disease, who have a readily measurable tricuspid regurgitant velocity by Doppler echocardiography. If possible, we will attempt to identify a cohort of HAPE susceptible patients. Participants will undergo evaluation both at sea level (baseline) and at high altitude. Baseline (low altitude) testing will be performed in Bangor, North Wales, UK, and will include evaluation of pulmonary artery systolic pressures, cardiac output, and oxygen saturation at rest and during submaximal exercise before and after inhalation of iloprost. This strategy will then be repeated at an altitude of approximately 5000 meters in the Dhaulagiri region of Nepal.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoxic Pulmonary Vasoconstriction
Keywords
To study the effects of iloprost on hypoxic pulmonary vasoconstriction at high altitude

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
iloprost
Other Intervention Name(s)
Ventavis (brand name)
Intervention Description
Baseline echo measurements, cardiac output, pulse oximetry will be taken. Subjects will then be given one dose of inhaled iloprost. Post-inhalation, the measurements will be repeated at rest and with exercise.
Primary Outcome Measure Information:
Title
Exercise capacity, pulmonary artery systolic pressure, cardiac output, oxygen saturation
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Heart rate, tissue Doppler echocardiographic measurements
Time Frame
6 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age: 18 - 80 years Healthy physically active males or females Have readily measurable tricuspid regurgitation (TR) peak systolic velocity by continuous wave Doppler ultrasound Exclusion Criteria: Unable to measure TR velocity Known liver disease Pregnancy Nitrates, cyclosporin, glyburide or other medications that in the opinion of the investigators could place subjects at increased risk of complications Any other medical condition that in the opinion of the investigators would place the subject at high risk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James D Anholm, MD
Organizational Affiliation
Jerry L. Pettis VA Mecial Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jerry L. Pettis VA Medical Center
City
Loma Linda
State/Province
California
ZIP/Postal Code
92357
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
James D Anholm, MD
Phone
909-583-6098
Email
James.Anholm@va.gov

12. IPD Sharing Statement

Learn more about this trial

Effects of Iloprost on Hypoxic Pulmonary Vasoconstriction and Exercise Capacity at High Altitude

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