Phase
Condition
Congestive Heart Failure
Hyponatremia
Heart Failure
Treatment
N/AClinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Previous clinical diagnosis of heart failure with preserved ejection fraction (ordiastolic heart failure) with current New York Heart association (NYHA) class II-IVsymptoms
Left ventricular ejection fraction (LVEF) greater than or equal to 50%, as determinedby echocardiography in the 12 months before study entry
Has experienced at least one of the following in the 12 months before study entry
Hospitalization for decompensated heart failure
Acute treatment with intravenous loop diuretics or hemofiltration
E/E' ratio greater than or equal to 15 measured by echocardiography
E/E' ratio greater than or equal to 8, and left atrial volume index (LAVI)greater than or equal to 40 ml/m2 measured by echocardiography
E/E' ratio greater than or equal to 8 measured by echocardiography, and plasmaBNP concentration greater or equal to 200 pg/ml
Exclusion
Exclusion Criteria:
History of reduced LVEF (less than 50%)
Valve disease (greater than mild stenosis or regurgitation)
Hypertrophic cardiomyopathy
Infiltrative or inflammatory myocardial disease
Pericardial disease
Obstructive or restrictive lung disease
Primary pulmonary arteriopathy
Has neuromuscular, orthopedic, or other non-cardiac condition that prevents individualfrom exercise testing
Has experienced myocardial infarction or unstable angina, or has undergonepercutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)within 60 days before study entry
Non-cardiac illness with estimated life expectancy less than 1 year at the time ofstudy entry, based on the judgment of the physician
Current use of nitrate therapy
Current use of other phosphodiesterase 5 inhibitors (ie. sildenafil, vardenafil,tadalafil) for treatment of impotence or pulmonary artery hypertension
Current use of cytochrome P450 3A4 inhibitors (ie. ketoconazole, itraconazole,erythromycin, saquinavir, cimetidine, protease inhibitors for HIV)
Severe hypotension (systolic blood pressure [SBP] less than 90mmHg or diastolic bloodpressure [DBP] less than 50mmHg) or uncontrolled hypertension (SBP greater than 180mmHg or DBP greater than 100mmHg)
Resting heart rate (HR) greater than 100bpm
Known severe renal dysfunction (estimated glomerular filtration rate [GFR] less than 30ml/min/1.73m2 by modified modification of diet in renal disease [MDRD] equation)
Known severe liver disease (alanine transaminase [ALT] or aspartate aminotransferase [AST] level greater than three times the upper normal limit, alkaline phosphatase [ALP] or total bilirubin greater than two times the upper normal limit)
History of leukemia, multiple myeloma or penile deformities that increase the risk forpriapism (eg. Peyronie's disease)
History of proliferative diabetic retinopathy, retinitis pigmentosa, nonischemic opticneuropathy, or unexplained visual disturbance
Female patients currently pregnant or women of childbearing age who were not usingcontraception
Listed for heart transplantation
Study Design
Study Description
Connect with a study center
Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do 463-707
Korea, Republic ofActive - Recruiting
Seoul National University Hospital
Seoul, 110-744
Korea, Republic ofActive - Recruiting

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