Clinical Trial

Safety and Effectiveness of the Peripheral Balloon-Expandable Covered Stent System for Iliac Artery Stenosis/Occlusion. (SELECT)

Study acronym: SELECT
Recruiting
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Record status
This record was last updated December 4, 2024 (before its estimated July 15, 2026 completion). Its status may not reflect the trial's current state.
Summary
This is a prospective, multi-center, single-arm clinical trial to evaluate the Peripheral Balloon-Expandable Covered Stent System for treating stenosis and/or occlusion in the common and external iliac arteries. The safety and effectiveness of the stent system will be compared to pre-set performance goals. All treated subjects will have follow-up visits at discharge, and at 1, 6, 12, 24, and 36 months after the procedure.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-09-17.
Status change: Not Yet Recruiting → Recruiting 2024-11-29
Trial Details
NCT Number NCT06605209
Lead Sponsor Zhejiang Zylox Medical Device Co., Ltd.
Conditions Peripheral Artery Disease (PAD)
Enrollment 130 participants
Start Date 2024-11-08
Primary Completion 2026-07-15 (estimated)
Study Completion 2026-12-15 (estimated)
Updated on ClinicalTrials.gov 2024-12-04