← Eichor
Study identifier: NCT06605209 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Peripheral Artery Disease (PAD)  ·  Sponsor: Zhejiang Zylox Medical Device Co., Ltd.

PhaseNA
Planned participants130
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Wei Guo, MD  ·  +86 010-66938349  ·  pla301dml@vip.sina.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First Medical Centre, Chinese PLA General HospitalBeijing, Beijing Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06605209