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Inhaled Iloprost, Dynamic Hyperinflation, and Oxidative Stress in COPD Patients

Inhaled Iloprost, Dynamic Hyperinflation, and Oxidative Stress in COPD Patients

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01941225
Enrollment
24
Registered
2013-09-13
Start date
2013-09-30
Completion date
2016-11-30
Last updated
2016-12-16

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

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

Chronic obstructive pulmonary disease, Pulmonary vasculature, Inhaled iloprost, Inhaled prostacyclin, Dynamic hyperinflation, Oxidative stress, Cardiopulmonary exercise testing, B-type natriuretic peptide

Brief summary

The purpose of this study is to investigate the role of the pulmonary vasculature in the development and progression of chronic obstructive pulmonary disease (COPD). To accomplish this, an inhaled prostacyclin (iloprost) will be given to patients with COPD and changes in oxidative stress and lung volumes during exercise will be measured.

Detailed description

Chronic obstructive pulmonary disease (COPD), the 3rd leading cause of death in the US, is a progressive disorder for which new treatments are urgently needed, as existing therapies are focused primarily on symptom relief. Oxidative stress, in part arising from inducible nitric oxide synthase (iNOS) released by the pulmonary vasculature, is critical for the development and progression of COPD; a treatment strategy focused on the pulmonary vasculature is hypothesized to be beneficial in COPD patients. This will be studied with the use of an inhaled prostacyclin analogue, iloprost, which has been approved for pulmonary hypertension and investigated in small studies of COPD patients. Potential mechanisms include reductions in dynamic hyperinflation during exercise in COPD patients or improvements in oxidative stress

Interventions

DRUGInhaled iloprost 5.0 mcg

Single administration

DRUGPlacebo

Single administration

Sponsors

Louisiana State University Health Sciences Center in New Orleans
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 40 years old or older * Physician diagnosis of chronic obstructive pulmonary disease * 10 or more pack-year smoking history * FEV1/FVC \<0.70 * FEV1 35-80% of predicted

Exclusion criteria

* Acute exacerbation of COPD within the last 30 days * Pregnant or breast-feeding * Contraindications to cardiopulmonary exercise testing * Known intolerance or allergy to iloprost * On oral corticosteroids (may be included if off for 7 days prior to testing) * Supplemental oxygen need * Known inflammatory disease other than COPD * Active solid organ/hematologic malignancy

Design outcomes

Primary

MeasureTime frameDescription
Dynamic hyperinflation during maximal cardiopulmonary exercise testAcute response (exercise testing performed 30 minutes after study drug administration)Dynamic hyperinflation will be measured as EELV/TLC ratio (end-expiratory lung volume/total lung capacity ratio) during exercise

Secondary

MeasureTime frameDescription
Blood markers of inflammationAcute response (measured 10 minutes, 30 minutes, 40 minutes, and 100 minutes after study drug administration)IL-1 beta, IL-6, IL-8, IL-10, IL-13, IL-18, TNF-alpha
Dead space fractionAcute response (measured every 2 minutes during exercise, starting 30 minutes after study drug administration)
B-type natriuretic peptideAcute response (measured 30 and 40 minutes after study drug administration)
Partial pressure of oxygenAcute response (measured 30 minutes after study drug administration and every 2 minutes during exercise)
Blood markers of oxidative stressAcute response (measured 10 minutes, 30 minutes, 40 minutes, and 100 minutes after study drug administration)8-isoprostane, superoxide dismutase, catalase, nitrite, malondialdehyde
Blood cyclic AMP levelsAcute response (measured 10 minutes, 30 minutes, 40 minutes, and 100 minutes after study drug administration)
Blood iloprost levelsAcute response (measured 10 minutes, 30 minutes, 40 minutes, and 100 minutes after study drug administration)
Exercise time and external work performedmeasured during exercise test 30 minutes after study drug administration
Borg dyspnea and leg scoresDuring exericse (starting 30 minutes after study drug administration)
Metabolic and gas exchange parameters during cardiopulmonary exercise testAcute response (throughout exercise, starting 30 minutes after study drug administration)

Countries

United States

Outcome results

None listed

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