# Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents

> **NCT01319812** · PHASE2 · COMPLETED · sponsor: **Biotronik, Inc.** · enrollment: 463 (actual)

## Conditions studied

- Peripheral Artery Disease
- Peripheral Vascular Disease

## Interventions

- **DEVICE:** Astron Stents
- **DEVICE:** Pulsar Stents

## Key facts

- **NCT ID:** NCT01319812
- **Lead sponsor:** Biotronik, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2011-07
- **Primary completion:** 2015-09
- **Final completion:** 2017-09-07
- **Target enrollment:** 463 (ACTUAL)
- **Last updated:** 2019-03-21


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01319812

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01319812, "Investigational Device Exemption Study to Determine the Safety and Efficacy of the Astron and Pulsar Stents". Retrieved via AI Analytics 2026-06-13 from https://api.ai-analytics.org/clinical/NCT01319812. Licensed CC0.

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