Status: Recruiting
Minima Stent System Post- Approval Study (PAS)
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.
Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: Renata MedicalUpdated: Oct 23, 2025Locations: 15
Eligibility criteria
The subject's legally authorized representative has been informed of the nature... [+1]
Active bloodstream infection requiring antibiotic therapy within 3 days prior to... [+11]