# Feasibility Study of the Vessel Restoration System (VRS) for the Treatment of Atherosclerotic Lesions in the Superficial Femoral Artery (SFA) and/or Popliteal Artery (PA) After Sub-optimal Percutaneous Transluminal Angioplasty (PTA) or Atherectomy: REACTIVATE I

> **NCT05455021** · NA · ACTIVE_NOT_RECRUITING · sponsor: **Alucent Biomedical** · enrollment: 50 (estimated)

## Conditions studied

- PAD - Peripheral Arterial Disease

## Interventions

- **COMBINATION_PRODUCT:** Vessel Restoration System (VRS)

## Key facts

- **NCT ID:** NCT05455021
- **Lead sponsor:** Alucent Biomedical
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** ACTIVE_NOT_RECRUITING
- **Start date:** 2021-11-15
- **Primary completion:** 2026-11-15
- **Final completion:** 2026-11-15
- **Target enrollment:** 50 (ESTIMATED)
- **Last updated:** 2024-01-16


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05455021

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05455021, "Feasibility Study of the Vessel Restoration System (VRS) for the Treatment of Atherosclerotic Lesions in the Superficial Femoral Artery (SFA) and/or Popliteal Artery (PA) After Sub-optimal Percutaneous Transluminal Angioplasty (PTA) or Atherectomy: REACTIVATE I". Retrieved via AI Analytics 2026-07-05 from https://api.ai-analytics.org/clinical/NCT05455021. Licensed CC0.

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