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Pulmonary Arterial Hypertension clinical trials

View clinical trials related to Pulmonary Arterial Hypertension.

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NCT ID: NCT03464864 Completed - Clinical trials for Pulmonary Arterial Hypertension

Pharmacokinetics, Safety and Tolerability of Treprostinil Inhalation Powder in Healthy Normal Volunteers

Start date: March 9, 2018
Phase: Phase 1
Study type: Interventional

A Dose-Rising Clinical Trial to Evaluate the Pharmacokinetics, Safety and Tolerability of Treprostinil Inhalation Powder in Healthy Normal Volunteers

NCT ID: NCT03422328 Completed - Clinical trials for Pulmonary Arterial Hypertension

A Clinical Study to Investigate the Long-term Safety of the Drug Macitentan in Patients With Pulmonary Hypertension Who Were Previously Treated With Macitentan in Clinical Studies.

UMBRELLA
Start date: April 5, 2018
Phase: Phase 3
Study type: Interventional

The aim of the trial is to study the long-term safety of macitentan and to provide continued treatment with macitentan to patients with pulmonary arterial hypertension (PAH) and Chronic thromboembolic pulmonary hypertension (CTEPH) who were previously treated with macitentan in clinical studies.

NCT ID: NCT03401476 Enrolling by invitation - Clinical trials for Pulmonary Arterial Hypertension

Effect of Morphine on Dyspnea and 6-Minute Walk Distance in Pulmonary Arterial Hypertension

Start date: May 8, 2017
Phase: Phase 2
Study type: Interventional

Despite advances in treatment and corresponding improvements in survival, patients with pulmonary arterial hypertension (PAH) remain highly symptomatic. In one survey of 315 patients with PAH, sixty-eight percent had moderate or severe dyspnea on exertion and 40% had a profound and clinically significant deficit in quality of life. Palliative care is being increasingly investigated in life-limiting cardiovascular diseases to alleviate symptoms. In PAH, its implementation is frequently delayed until end-of-life. Opioids are a common palliative care intervention, however the efficacy and safety of opioids for symptom relief in PAH has not been evaluated.

NCT ID: NCT03365479 Completed - Clinical trials for Pulmonary Hypertension

Acute Response of Iloprost Inhalation Using the Breelib Nebulizer in Pulmonary Arterial Hypertension

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Primary objective • To evaluate the effect of rapid inhalation of 2.5μgiloprost using the Breelib nebulizer on pulmonary vascular resistance (PVR) in patients with pulmonary arterial hypertension Secondary objectives - To evaluate the effect of rapid iloprost inhalation using the Breelib nebulizer on mean pulmonary arterial pressure (mPAP), cardiac output (CO), cardiac index (CI), systemic blood pressure, arterial oxygen saturation, heart rate, and pulmonary arterial wedge pressure (PAWP). - To evaluate the safety and tolerability of the rapid iloprost inhalation using the Breelib nebulizer.

NCT ID: NCT03364244 Completed - Clinical trials for Pulmonary Arterial Hypertension

Revatio Special Investigation for Long-term Use in Pediatric Patients

Start date: November 30, 2017
Phase:
Study type: Observational

Secondary data collection study: safety and effectiveness of Revatio in pediatric patients under Japanese medical practice

NCT ID: NCT03362047 Recruiting - Clinical trials for Pulmonary Arterial Hypertension (PAH)

(RIGHT HEART III Study - Right Ventricular Hemodynamic Evaluation and Response to Treatment)

RightHeartIII
Start date: March 1, 2018
Phase: Phase 2
Study type: Interventional

Pilot study to determine the therapeutic effect of two prarallel groups treated with either Riciguat or Macitentan, evaluated by the change in systolic and diastolic RV function within 12 weeks after first drug intake in order to plan a larger Phase II study.

NCT ID: NCT03344159 Completed - Clinical trials for Pulmonary Arterial Hypertension

Spironolactone Therapy in Chronic Stable Right HF Trial

STAR-HF
Start date: April 1, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety, tolerability and mechanistic effects of spironolactone, an aldosterone receptor antagonist, on sympathetic nervous system activity and right heart function and remodeling in patients with chronic right heart failure.

NCT ID: NCT03315507 Completed - Clinical trials for Pulmonary Arterial Hypertension

A Study to Assess the Safety, Tolerability, and Hemodynamic Response of PB1046 in Subjects With PAH

Start date: October 20, 2017
Phase: Phase 1
Study type: Interventional

PB1046-PT-CL-0005 is an open-label, dose-titration study to assess the safety, tolerability, and hemodynamic effects of individually dose-titrated PB1046 administered by weekly subcutaneous injection for 8 weeks in adult subjects with PAH who have a permanently implanted hemodynamic monitor in the distal pulmonary artery. The primary objectives of the study are to assess the overall safety, tolerability, and hemodynamic profile of a PB1046 across an individually titrated dose range.

NCT ID: NCT03288025 Active, not recruiting - Insulin Resistance Clinical Trials

Pulmonary Arterial Hypertension Improvement With Nutrition and Exercise (PHINE)

Start date: September 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the extent to which diet and exercise may improve PAH through the modulation of insulin sensitivity. The central hypothesis is that dysregulated glucose metabolism elicits a response in PAH patients that can be modified by exercise and diet, thereby leading to improvements in pulmonary vascular disease.

NCT ID: NCT03282266 Completed - Clinical trials for Pulmonary Arterial Hypertension

Safety and Efficacy of Pulmonary Artery Denervation in Patients With Pulmonary Arterial Hypertension

PADN-CFDA
Start date: January 18, 2018
Phase: N/A
Study type: Interventional

The objective of this randomized control trial is to gain clinical insight on the use of pulmonary artery denervation (PADN) for the treatment of pulmonary arterial hypertension (PAH). The primary objective is to assess effectiveness and safety of PADN for the treatment of PAH.