Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Pulmonary Arterial Hypertension
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

This is a multi-national, multi-center, prospective, non-randomized, open label trial of patients implanted with the study device. A total of 20 patients will be implanted with the study device and followed at regular intervals for 1 year and then annually for a total of 5 years post implant.

This is a multi-national, multi-center, prospective, non-randomized, open label trial of patients implanted with the study device. A total of 20 patients will be implanted with the study device and followed at regular intervals for 1 year and then annually for a total of 5 years post implant.

Tracking Information

NCT #
NCT03838445
Collaborators
Not Provided
Investigators
Principal Investigator: Victor Tapson, M.D. Cedars-Sinai Medical Center