Viewing Study NCT02554903



Ignite Creation Date: 2024-05-06 @ 7:33 AM
Last Modification Date: 2024-10-26 @ 11:49 AM
Study NCT ID: NCT02554903
Status: COMPLETED
Last Update Posted: 2021-04-01
First Post: 2015-09-08

Brief Title: Clinical Study to Assess the Efficacy and Safety of Macitentan in Patients With Pulmonary Hypertension After Left Ventricular Assist Device Implantation
Sponsor: Actelion
Organization: Actelion

Study Overview

Official Title: A Prospective Multicenter Double-blind Randomized Placebo-controlled Parallel Group Study to Assess the Efficacy and Safety of Macitentan in Patients With Pulmonary Hypertension After Left Ventricular Assist Device Implantation
Status: COMPLETED
Status Verified Date: 2021-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SOPRANO
Brief Summary: STUDY OBJECTIVES Primary objective To evaluate the effect of macitentan 10 mg on pulmonary vascular resistance PVR as compared to placebo in subjects with pulmonary hypertension PH after left ventricular assist device LVAD implantation

Secondary objectives To evaluate the effect of macitentan 10 mg as compared to placebo on cardio-pulmonary hemodynamics and disease severity in subjects with PH after LVAD implantation

To evaluate the safety and tolerability of macitentan 10 mg in subjects with PH after LVAD implantation

Exploratory objectives To explore the potential effect of macitentan 10 mg as compared to placebo on right ventricular function in subjects with PH after LVAD implantation

To explore the potential effect of macitentan 10 mg as compared to placebo on selected clinical events in subjects with PH after LVAD implantation

To explore the potential effect of macitentan 10 mg as compared to placebo on renal function as measured by glomerular filtration rate GFR in subjects with PH after LVAD implantation
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None