Viewing StudyNCT02826252



Ignite Creation Date: 2024-05-06 @ 8:47 AM
Last Modification Date: 2024-10-26 @ 12:05 PM
Study NCT ID: NCT02826252
Status: COMPLETED
Last Update Posted: 2017-03-15
First Post: 2016-07-05

Brief Title: Examination of Ventavis Iloprost Inhalation Behavior Using the I-Neb AAD System in Patients With Pulmonary Arterial Hypertension When Switching the Iloprost Nebulizer Solution for Inhalation From 10 μgmL V10 to 20 μgmL V20
Sponsor:
Organization: Bayer

Study Design

Study Type: OBSERVATIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: False
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 64
Enrollment Type: ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
Name
Case-Crossover
Time Perspective List:

Clinical Trial Statuses

Name
35675
Who Masked List: