Last updated: February 13, 2024
Sponsor: University of Oklahoma
Overall Status: Completed
Phase
N/A
Condition
High Blood Pressure (Hypertension)
Diabetes And Hypertension
Congestive Heart Failure
Treatment
iloprost Inhalation
iloprost
Clinical Study ID
NCT00561223
1024
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- FEV1 < 65% of predicted and FEV1 to FVC ratio < 70%
- Baseline PAO2 while stable between 60-75 mmHg and
- The ability to provide informed consent
Exclusion
Exclusion Criteria:
- Clinical instability as evidenced by an acute exacerbation requiring anintensification of therapy and/or the need for hospitalization with the preceding 3months.
- Presence of an additional cause of lung disease as suggested by history, clinical orradiographic findings, or pulmonary function tests
- Presence of left ventricular dysfunction and/or left atrial enlargement by echo, ECHOor catheterization
- Heparin allergy
- Pregnancy or breast feeding
Study Design
Total Participants: 10
Treatment Group(s): 2
Primary Treatment: iloprost Inhalation
Phase:
Study Start date:
November 01, 2006
Estimated Completion Date:
October 31, 2012
Study Description
Connect with a study center
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma 73104
United StatesSite Not Available

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