U.S., Feb. 15 -- ClinicalTrials.gov registry received information related to the study (NCT06828770) titled 'Minima Stent System Post- Approval Study (PAS)' on Feb. 03.
Brief Summary: This Post-Approval Study is a single arm, prospective, multi-center, open-label study of patients treated with the Renata Minima Stent System in the United States. The objective of the study is to continue the assessment of device performance and capture outcome data on use of the device in real-world use.
Study Start Date: March, 2025
Study Type: OBSERVATIONAL
Condition:
Pulmonary Artery Stenosis
Aortic Coarctation
Intervention:
DEVICE: Minima Stent System
Minima Stent System is indicated for use in the treatment of native or acquired pulmonary artery...