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Pulmonary Hypertension clinical trials

View clinical trials related to Pulmonary Hypertension.

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NCT ID: NCT01156636 Completed - Clinical trials for Pulmonary Hypertension

Phosphodiesterase-5 (PDE5) Inhibition and Pulmonary Hypertension in Diastolic Heart Failure

Start date: January 2006
Phase: Phase 2/Phase 3
Study type: Interventional

Prevalence of heart failure (HF) with left ventricular (LV) diastolic dysfunction and preserved ejection fraction (EF) (HFpEF) is increasing. Prognosis worsens with development of pulmonary vasoconstriction and hypertension (PH) and right ventricular (RV) failure. The investigators aimed at modulating pulmonary vascular tone and RV burden in HFpEF due to high blood pressure (HBP), by using the phosphodiesterase-5 (PDE5) inhibitor sildenafil.

NCT ID: NCT01135706 Completed - Clinical trials for Pulmonary Hypertension

Fractal Analysis of the Pulmonary Arterial Tree in Pulmonary Hypertension

Start date: April 2010
Phase: N/A
Study type: Observational

The investigators propose to confirm that normotensive and hypertensive pulmonary arteries are fractal, as well as define if the FD correlates to disease severity when compared to available data such as six-minute walk and right heart catheterization measurements.

NCT ID: NCT01104870 Completed - Clinical trials for Pulmonary Hypertension

A Dose Response Study of UT-15C SR in Patients With Exercise-Induced Pulmonary Hypertension

Start date: April 2010
Phase: Phase 2
Study type: Interventional

This is a prospective, randomized, parallel group study to assess the hemodynamic effect of three different dose regimens of a sustained release (SR) tablet of UT-15C in patients with exercise-induced pulmonary hypertension (PH), as measured by the change in peak total pulmonary resistance index (TPRI) during exercise from Baseline to Week 12.

NCT ID: NCT01100008 Completed - Clinical trials for Pulmonary Hypertension

Cardiac Magnetic Resonance Imaging and Pulmonary Perfusion

Start date: September 2007
Phase: N/A
Study type: Interventional

Pulmonary hypertension is a rare severe disease leading to cardiac insufficiency. Treatment depends on the severity of the disease. This study evaluates cardiac MRI for the assessment of pulmonary hypertension severity and identification of parameters useful for the follow-up in order to adapt the medical treatment to status of the patient. Evaluate if cardiac MRI can obviate right cardiac catheterization in the follow-up.

NCT ID: NCT01076296 Completed - Clinical trials for Pulmonary Hypertension

A Post-Marketing Study for On Label Evaluation of the GE Vscan Ultrasound Imaging System

Start date: February 2010
Phase: N/A
Study type: Observational

This study is to collect data and learn more about the Vscan Ultrasound Imaging System. It is an "observational" study with no additional procedures or intervention prescribed other than using the Vscan along with a routine medical physical exam.

NCT ID: NCT01062282 Completed - Clinical trials for Pulmonary Hypertension

Hypertension Study of Ventavis® Inhalation Therapy in the Treatment of Patients With Pulmonary Arterial Hypertension (VENIS)

Start date: July 2006
Phase: N/A
Study type: Observational

The purpose of this study is to gain information on safety and efficacy from Korean patients who starting Ventavis treatment by observational method.

NCT ID: NCT01055405 Completed - COPD Clinical Trials

Study of Sildenafil Effects in Combination With Rehabilitation in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Associated Pulmonary Hypertension

SIL-COPD-02
Start date: August 2008
Phase: Phase 4
Study type: Interventional

Sildenafil is a phosphodiesterase-5 inhibitor that has been approved for the treatment of pulmonary arterial hypertension with orphan drug designation. Sildenafil modulates the nitric oxide (NO) pathway in the vessel wall. Since this pathway is impaired in pulmonary arteries of patients with pulmonary hypertension (PH) associated with chronic obstructive pulmonary disease (COPD), the investigators hypothesized that sildenafil might improve pulmonary hemodynamics and increase exercise tolerance in this condition.

NCT ID: NCT01051960 Completed - Clinical trials for Pulmonary Hypertension

Exercise Induced Pulmonary Hypertension in Systemic Sclerosis and Treatment With Ambrisentan

Start date: March 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the clinical characteristics and hemodynamic profiles that predict exercise induced pulmonary hypertension in 15 patients with systemic sclerosis. The study also aims to determine the effectiveness of Ambrisentan for subjects with exercise induced Pulmonary Arterial Hypertension (PAH) with scleroderma

NCT ID: NCT01048905 Completed - Sickle Cell Disease Clinical Trials

Glutamine Therapy for Hemolysis-Associated Pulmonary Hypertension

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The primary hypothesis of this study is that glutamine supplementation will improve the erythrocyte glutamine/glutamate ratio, a biomarker of oxidative stress, hemolysis and pulmonary hypertension (PH) in sickle cell disease (SCD) and thalassemia (Thal) patients with PH. PH is defined as a tricuspid regurgitant jet velocity (TRV) on Doppler echocardiography > 2.5 m/s. We also predict that glutamine therapy will increase arginine bioavailability and subsequently alter sickle red cell endothelial interaction that can be identified using endo-PAT technology through nitric oxide (NO) generation, leading to changes in biological markers, and clinical outcome. Specifically our second hypothesis is that oral glutamine will decrease biomarkers of hemolysis and adhesion molecules, and improve the imbalanced arginine-to-ornithine ratio that occurs in hemolytic anemias, leading to improved arginine bioavailability and clinical endpoints of endothelial dysfunction and PH in patients with SCD and Thal.

NCT ID: NCT01028651 Completed - Clinical trials for Pulmonary Hypertension

A Study to Assess the Safety and Efficacy of Treprostinil to Facilitate Liver Transplantation in Patients With Portopulmonary Hypertension

Start date: November 2009
Phase: N/A
Study type: Observational

This is a multicenter, observational, open-label study. Patients meeting inclusion/exclusion criteria will receive treatment with treprostinil as recommended by their treating physician and will follow patients according to standard of care. This observational study proposes to collect clinical data and biologic specimens from patients who will be treated for Portopulmonary Hypertension, with a goal of achieving hemodynamic parameters acceptable for liver transplantation.