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Pulmonary Hypertension clinical trials

View clinical trials related to Pulmonary Hypertension.

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NCT ID: NCT04636892 Recruiting - Clinical trials for Coronary Artery Disease

Evaluating Infrasonic Hemodynography

Start date: January 4, 2021
Phase: N/A
Study type: Interventional

This comparative diagnostic accuracy study will determine the accuracy of a noninvasive wearable infrasonic sensor to detect the mechanical, electrical, and hemodynamic function of the cardiovascular system.

NCT ID: NCT04633538 Completed - Clinical trials for Pulmonary Hypertension

Evaluation of a New 6 Minute Walk Test Smartphone App in Patients With Pulmonary Hypertension

6-APP
Start date: January 15, 2018
Phase:
Study type: Observational

Comparison of standard 6 minute walk test with 6 minute walk test smartphone app.

NCT ID: NCT04624490 Recruiting - Asthma Clinical Trials

Hyperpolarized 129Xe MR Imaging of Lung Function in Healthy Volunteers and Subjects With Pulmonary Disease

Start date: November 2, 2020
Phase: Phase 1
Study type: Interventional

The purpose of this study is to develop and evaluate the usefulness of hyperpolarized (HP) 129Xe gas MRI for regional assessment of pulmonary function.

NCT ID: NCT04623528 Completed - Clinical trials for Pulmonary Hypertension

Characterization of the Liver Parenchyma Using Parametric T1 and T2 Magnetic Resonance Relaxometry

Start date: January 2014
Phase:
Study type: Observational

- To determine normal T1 and T2 values of the liver, and to assess the impact of age and gender - To determine the relation between markers of right heart decompensation and T1/T2 values of the liver in patients with pulmonary hypertension, patients with dilated cardiomyopathy, and patients with constrictive pericarditis (or constrictive physiology) - To determine inter/intra-observer reproducibility for liver T1/T2 assessment - To test/develop multi-feature texture analysis for T1/T2 analysis of the liver and implement machine learning to derive indicative features (MR-derived measures only vs combined with other clinical readouts)

NCT ID: NCT04615754 Completed - Clinical trials for Pulmonary Hypertension

Ketones for Pulmonary Hypertension - Effects on Hemodynamics

KEPAH
Start date: August 18, 2020
Phase: Phase 2
Study type: Interventional

In the present study, patients with idiopathic pulmonary hypertension (IPAH) and chronic thromboembolic pulmonary hypertenion will be investigated in a randomized cross-over design with ketone infusions and placebo. Invasive and non-invasive hemodynamics will be evaluated

NCT ID: NCT04594629 Recruiting - Clinical trials for Pulmonary Hypertension

PGI2 Versus Nitroglycerine for Management of Pulmonary Hypertension After Valve Surgeries

Start date: November 2020
Phase: Phase 1
Study type: Interventional

This study was conducted in 120 patients aged from 54-65 years scheduled for elective valve replacement surgeries. Patients were randomly allocated to nitro glycerine or PGI2 groups. Patients of nitro glycerine group received nebulized nitro glycerine at a rate of 2.5-5 mcg/kg/min (5 mg, 1 mg/ml) over 10 minutes by ultrasonic nebuliser. Patients of PGI2 group received nebulized PGI2 (epoprostenol), 20000 ng/ml (20000 ng/ml in 60 ml syringe was attached to an intravenous pump which delivers a titrating rate of 8 ml/h . The primary outcome was mean pulmonary artery pressure. The secondary outcomes included mean arterial blood pressure (MAP) (mmHg), PaO2/FiO2 ratio, cardiac index (CI) (l/min/m2) right ventricular ejection fraction (RVEF), central venous pressure(CVP) , 30-day mortality rate and the incidence of complications such as facial flushing, hypotension and re-exploration for bleeding.

NCT ID: NCT04589390 Recruiting - Clinical trials for Pulmonary Hypertension

Selexipag for the Treatment of Schistosomiasis-Associated Pulmonary Arterial Hypertension

SELSCH
Start date: October 15, 2020
Phase: Phase 2
Study type: Interventional

Pulmonary arterial hypertension (PAH) is a severe, progressive and potentially fatal disease that impairs the pulmonary circulation and leads to right ventricular failure. One of the world most prevalent etiologies of PAH is schistosomiasis-associated pulmonary arterial hypertension (Sch-PAH). New drugs have emerged to treat other forms of PAH, but their benefits cannot be automatically translated for Sch-PAH patients, since this etiology was not included in the pivotal PAH trials. One of the most promising therapies for the treatment of PAH to emerge in recent years is selexipag, an oral IP receptor agonist, which acts on the prostacyclin pathway. The present study aims to evaluate the efficacy, safety and tolerability of selexipague for the treatment of schistosomiasis-associated pulmonary arterial hypertension.

NCT ID: NCT04578223 Completed - Clinical trials for Pulmonary Hypertension

Platelet Reactivity and Treatment With Prostacyclin Analogues in Pulmonary Arterial Hypertension

PAPAYA
Start date: July 5, 2017
Phase:
Study type: Observational

Background: Prostacyclin analogues (epoprostenol, treprostinil and iloprost) induce vasodilation in advanced pulmonary arterial hypertension (PAH) but also inhibit platelets, increasing patients' bleeding risk. The antiplatelet effects of different prostacyclin analogues have never been compared head-to-head. The goal of the PAPAYA (Platelet Reactivity and Treatment With Prostacyclin Analogues in Pulmonary Arterial Hypertension) trial is(i) to compare platelet function (platelet reactivity, extracellular vesicles concentration and thrombus formation) in patients with PAH treated with prostacyclin analogues on top of endothelin receptor antagonists (ERA) and/or phosphodiesterase type 5 inhibitors (PDE5i) and patients treated only with ERA and PDE5i, and (ii) to compare the antiplatelet effect of different prostacyclin analogues. Venous blood will be collected from patients treated with prostacyclin analogues (study group; n=40) and patients treated with ERA or PDE5i (control group; n=40). Platelet reactivity will be analysed in whole blood by impedance aggregometry using arachidonic acid, adenosine diphosphate and thrombin receptor-activating peptide as agonists. Concentrations of extracellular vesicles from all platelets (CD61+), activated platelets (CD62P+), leukocytes (CD45+) and endothelial cells (CD146+) will be analysed in platelet-depleted plasma using flow cytometry (A-60 Micro). Platelet-rich thrombus formation will be measured using whole blood perfusion system. The study will determine the antiplatelet effect of prostacyclin analogues and compare different prostacyclin analogues head-to-head to identify the best drugs to use in case of thrombosis or bleeding.

NCT ID: NCT04559516 Withdrawn - Clinical trials for Pulmonary Hypertension

Remote Exercise Program Delivery Using a Mobile Application for Pulmonary Arterial Hypertension

REVAMP
Start date: November 3, 2022
Phase: N/A
Study type: Interventional

This study will determine the feasibility of a mobile application-based home exercise rehabilitation program for patients with pulmonary hypertension.

NCT ID: NCT04555161 Recruiting - Clinical trials for Pulmonary Hypertension

Treatment of Pulmonary Arterial Hypertension Using the Aria CV Pulmonary Hypertension System

ASPIRE PH
Start date: March 15, 2021
Phase: N/A
Study type: Interventional

This prospective study is a multi-center early feasibility study assessing the safety and performance of the Aria CV Pulmonary Hypertension System in patients with pulmonary hypertension and right heart dysfunction.