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Acute Assessment of the Aria CV System in Patients With WHO Groups 2 and 3 Pulmonary Hypertension

Pulmonary Hypertension Clinical Trial

Official title:
Acute Feasibility Study Assessing Safety and Performance of Aria CV Acute PH System in Patients With WHO Group 2 and 3 Pulmonary Hypertension

Clinical Trial Summary

This study is a prospective, non-randomized, two arm, single-center acute feasibility study assessing safety and performance of the Aria CV Acute PH System in WHO Group 2 and 3 PH patients.

Clinical Trial Description

This study is a prospective, non-randomized, two arm, single-center acute feasibility study assessing safety and performance of the Aria CV Acute PH System in WHO Group 2 and 3 PH patients. The planned enrollment is a maximum enrollment of 40 patients to ensure up to 10 "Device Deployed" subjects in each arm at one site. The duration of study participation for each subject is expected to be approximately 60 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05001711
Study type Interventional
Source Aria CV, Inc
Contact
Status Completed
Phase N/A
Start date July 12, 2021
Completion date January 6, 2022
View Details
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