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 — REACTIVATE I

PAD - Peripheral Arterial Disease Clinical Trial

Official title:
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

Status Active, not recruiting

Clinical Trial Summary

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

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

PAD - Peripheral Arterial Disease
Peripheral Arterial Disease
Peripheral Vascular Diseases

Clinical Trial Details

NCT number	NCT05455021
Study type	Interventional
Source	Alucent Biomedical
Contact
Status	Active, not recruiting
Phase	N/A
Start date	November 15, 2021
Completion date	November 15, 2026

View Details

See also
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