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RecruitingNCT06075940

Evaluation of the MAGNITUDE® Bioresorbable Drug-Eluting Scaffold in the Treatment of Patients With Below the Knee Disease in Australia

Evaluation of the MAGNITUDE® Bioresorbable Drug-Eluting Scaffold (BRS)in the Treatment of Patients With Below the Knee Disease in Australia

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
R3 Vascular Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this prospective, multi-center, clinical investigation is to evaluate the MAGNITUDE BRS System for the planned treatment of narrowed infrapopliteal lesions. Up to 30 subjects will be enrolled at approximately 3 clinical sites in Australia.

Conditions

Interventions

TypeNameDescription
DEVICEMAGNITUDE BRSTreatment with the MAGNITUDE Scaffold

Timeline

Start date
2024-03-04
Primary completion
2026-12-31
Completion
2030-12-31
First posted
2023-10-10
Last updated
2024-04-10

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT06075940. Inclusion in this directory is not an endorsement.

Evaluation of the MAGNITUDE® Bioresorbable Drug-Eluting Scaffold in the Treatment of Patients With Below the Knee Diseas (NCT06075940) · Clinical Trials Directory