Sildenafil to Increase Exercise Capacity in Individuals With Idiopathic Pulmonary Fibrosis and Pulmonary Hypertension
Status: | Completed |
---|---|
Conditions: | High Blood Pressure (Hypertension), High Blood Pressure (Hypertension), Pulmonary |
Therapuetic Areas: | Cardiology / Vascular Diseases, Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 19 - Any |
Updated: | 7/30/2016 |
Start Date: | November 2004 |
End Date: | July 2007 |
Sildenafil Treatment in Patients With Idiopathic Pulmonary Fibrosis and Pulmonary Hypertension - a Pilot Cross-over Study
Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease that affects an individual's
ability to breathe. Currently, no medications can reverse the damage to the lungs caused by
IPF, but individuals are encouraged to engage in moderate exercise to strengthen lung
function. This study will evaluate the effectiveness of sildenafil at improving exercise
tolerance and breathing difficulties in individuals with IPF.
ability to breathe. Currently, no medications can reverse the damage to the lungs caused by
IPF, but individuals are encouraged to engage in moderate exercise to strengthen lung
function. This study will evaluate the effectiveness of sildenafil at improving exercise
tolerance and breathing difficulties in individuals with IPF.
IPF is a disease that damages the air sacs in the lungs and leads to widespread and
permanent scarring of lung tissue. Individuals with IPF may experience breathing
difficulties, cough, chest pain, and a decreased exercise capacity. There is no cure for
this disease, and individuals usually die within 3 to 5 years. It is recommended that
individuals with IPF engage in moderate exercise, as this can help maintain strength and
improve lung function. Many individuals with IPF also suffer from pulmonary hypertension,
which is high blood pressure in the arteries leading to the lungs. Sildenafil, a medication
currently used to treat pulmonary hypertension, increases blood flow to the lungs and
enhances gas exchange within the lungs. The purpose of this study is to evaluate the
effectiveness of sildenafil at improving exercise tolerance and breathing difficulties in
individuals with IPF and pulmonary hypertension.
This 3-week study will enroll individuals with IPF and pulmonary hypertension. Study visits
will occur at baseline, and Weeks 1 and 2. At the baseline visit, participants will perform
a 6-minute walk test, which will measure the distance walked in a 6-minute period. Oxygen
levels will be measured prior to and during the test, and standardized questionnaires will
be completed to assess breathing difficulties. A second 6-minute walk test will be performed
1 hour following the first test. At the Week 1 visit, participants will be randomly assigned
to receive a single dose of either 50 mg of sildenafil or placebo. One hour after receiving
the medication, they will complete another 6-minute walk test. The Week 2 visit will be
identical to the Week 1 visit, except participants who received sildenafil at Week 1 will
receive placebo at Week 2, and vice versa.
permanent scarring of lung tissue. Individuals with IPF may experience breathing
difficulties, cough, chest pain, and a decreased exercise capacity. There is no cure for
this disease, and individuals usually die within 3 to 5 years. It is recommended that
individuals with IPF engage in moderate exercise, as this can help maintain strength and
improve lung function. Many individuals with IPF also suffer from pulmonary hypertension,
which is high blood pressure in the arteries leading to the lungs. Sildenafil, a medication
currently used to treat pulmonary hypertension, increases blood flow to the lungs and
enhances gas exchange within the lungs. The purpose of this study is to evaluate the
effectiveness of sildenafil at improving exercise tolerance and breathing difficulties in
individuals with IPF and pulmonary hypertension.
This 3-week study will enroll individuals with IPF and pulmonary hypertension. Study visits
will occur at baseline, and Weeks 1 and 2. At the baseline visit, participants will perform
a 6-minute walk test, which will measure the distance walked in a 6-minute period. Oxygen
levels will be measured prior to and during the test, and standardized questionnaires will
be completed to assess breathing difficulties. A second 6-minute walk test will be performed
1 hour following the first test. At the Week 1 visit, participants will be randomly assigned
to receive a single dose of either 50 mg of sildenafil or placebo. One hour after receiving
the medication, they will complete another 6-minute walk test. The Week 2 visit will be
identical to the Week 1 visit, except participants who received sildenafil at Week 1 will
receive placebo at Week 2, and vice versa.
Inclusion Criteria:
- IPF, diagnosed according to the American Thoracic Society (ATS) and European
Respiratory Society (ERS) consensus statement (with or without surgical lung biopsy)
- Pulmonary hypertension, defined as mean pulmonary artery pressure (MPAP) greater than
or equal to 25 mm Hg by right heart catheterization (RHC)
Exclusion Criteria:
- Interstitial lung disease due to conditions other than IPF
- Recent lung or upper respiratory tract infection within 4 weeks of study entry
- Acute or chronic impairment other than dyspnea (e.g., angina pectoris, intermittent
claudication) limiting the ability to comply with study requirements (e.g., 6-minute
walk test)
- Known hypersensitivity to sildenafil
- Known or suspected coronary artery disease (CAD)
- Unstable angina
- Nitrate use
- Known or suspected aortic stenosis (AS)
- Known or suspected heart attack, stroke, or life-threatening arrythmias within 1
month of study entry
- Severe chronic heart failure, defined as New York Heart Association (NYHA) class
III/IV and/or left ventricular ejection fraction less than 25%
- Known penile deformities
- Known kidney or liver dysfunction
- Uncontrolled diabetes (blood glucose less than 60 mg/dl or greater than 300 mg/dl)
- Severe serum sodium abnormalities (serum sodium less than 130 mEq/L or greater than
150 mEq/L)
- Condition that may predispose participant to priapism (e.g., sickle cell anemia,
multiple myeloma, leukemia)
- Retinitis pigmentosa
- Known or suspected idiopathic hypertrophic subaortic stenosis (IHSS)
- Low blood pressure (systolic blood pressure [SBP] less than 100 mm Hg or diastolic
blood pressure [DBP] less than 50 mm Hg)
- Uncontrolled systemic high blood pressure (SBP greater than 180 mm Hg or DBP greater
than 100 mm Hg)
- Cardiopulmonary rehabilitation program started within 8 weeks of study entry or
likely to start prior to the conclusion of the study
- Treatment with an endothelin receptor antagonist, iloprost, epoprostenol, inhibitors
of CYP3A4 (e.g., cimetidine, erythromycin, ketoconazole, itraconazole, mibefradil),
protease inhibitors (e.g., amprenavir, indinavir, or ritonavir), rifampin,
alpha-blockers (e.g., doxazosin), or other phosphodiesterase-5 inhibitors
- Current use of alcohol, grapefruit juice, or St. John's wort
- Pregnant or breastfeeding
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