NCT05372952

An Investigator Initiated Trial to Evaluate the Safety and Feasibility of the DyNETIC-35 Stent for Iliac Lesions Via a Trans-radial Approach

An Investigator Initiated Trial to Evaluate the Safety and Feasibility of the DyNETIC-35 Cobalt Chromium Balloon-expandable Stent for the Treatment of Atherosclerotic Iliac Lesions Via a Trans-radial Approach - Bionetic-TRA

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 25 (actual)
• Sponsor: Klinikum Arnsberg · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This feasibility study with a 30 day follow up period will assess the safety and feasibility of the Dynetic-35 stent for the treatment of peripheral iliac artery lesions via a trans-radial approach.

Conditions

• Peripheral Arterial Disease

Interventions

Type	Name	Description
DEVICE	Dynetic-35 Peripheral Balloon-Expandable Stent System	Stenotic iliac lesions will be treated with the Dynetic 35 stent via a radial access

Timeline

• Start date: 2022-07-25
• Primary completion: 2025-06-03
• Completion: 2025-06-03
• First posted: 2022-05-13
• Last updated: 2026-01-23

Locations

1 site across 1 country: Germany