# Evaluation of Safety and Efficacy of the S.M.A.R.T. RADIANZ™ Vascular Stent System in the Treatment of Iliac and Femoropopliteal Lesions Via Transradial Access

> **NCT05399680** · NA · COMPLETED · sponsor: **Cordis US Corp.** · enrollment: 151 (actual)

## Conditions studied

- Peripheral Arterial Disease

## Interventions

- **DEVICE:** S.M.A.R.T. RADIANZ™ Vascular Stent System
- **DEVICE:** BRITE TIP RADIANZ™ Guiding Sheath
- **DEVICE:** SABERX RADIANZ™ PTA Balloon Catheter

## Key facts

- **NCT ID:** NCT05399680
- **Lead sponsor:** Cordis US Corp.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2022-06-29
- **Primary completion:** 2023-09-22
- **Final completion:** 2023-11-13
- **Target enrollment:** 151 (ACTUAL)
- **Last updated:** 2025-08-11

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05399680

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05399680, "Evaluation of Safety and Efficacy of the S.M.A.R.T. RADIANZ™ Vascular Stent System in the Treatment of Iliac and Femoropopliteal Lesions Via Transradial Access". Retrieved via AI Analytics 2026-06-26 from https://api.ai-analytics.org/clinical/NCT05399680. Licensed CC0.

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