# Post-Market Clinical Follow-Up of S.M.A.R.T. Family of Stents in Treating Iliac and Femoropopliteal Artery Disease

> **NCT07338890** · — · NOT_YET_RECRUITING · sponsor: **Cordis US Corp.** · enrollment: 240 (estimated)

## Conditions studied

- Superficial Femoral Artery Stenosis
- Iliac Artery Stenosis
- Popliteal Artery Stenosis

## Interventions

- **DEVICE:** S.M.A.R.T.™ Nitinol Stent System (SMART 120/150)
- **DEVICE:** S.M.A.R.T.™ CONTROL ™ Nitinol Stent System
- **DEVICE:** S.M.A.R.T.™ Flex Vascular Stent System

## Key facts

- **NCT ID:** NCT07338890
- **Lead sponsor:** Cordis US Corp.
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-01-31
- **Primary completion:** 2026-05-30
- **Final completion:** 2026-05-30
- **Target enrollment:** 240 (ESTIMATED)
- **Last updated:** 2026-01-14

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07338890

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07338890, "Post-Market Clinical Follow-Up of S.M.A.R.T. Family of Stents in Treating Iliac and Femoropopliteal Artery Disease". Retrieved via AI Analytics 2026-06-24 from https://api.ai-analytics.org/clinical/NCT07338890. Licensed CC0.

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