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Clinical Trial Summary

The stent-FP study investigates the impact of coverage of profound femoral artery (PFA) by bare metal stent deployed in proximal superficial femoral artery (SFA) lesions. 300 patients with femoral bifurcation lesions will be included and divided into 3 groups according to the location of proximal stent edge. The primary endpoint of the study is major adverse events and freedom from target lesion revascularization at 48 months. Secondary endpoints include primary patency of PFA and bare metal stent at 1,6, 12,24,36and 48 month, MAE and F -TLR at 1,6, 12,24,36 month.


Clinical Trial Description

n/a


Study Design


NCT number NCT04713865
Study type Observational
Source Qingdao Hiser Medical Group
Contact
Status Not yet recruiting
Phase
Start date August 18, 2021
Completion date August 17, 2026