Varithena Versus Endothermal Ablation of the Great Saphenous Vein (VERITAS)

PHASE4TerminatedINTERVENTIONAL
Enrollment

43

Participants

Timeline

Start Date

February 10, 2023

Primary Completion Date

April 4, 2024

Study Completion Date

April 4, 2024

Conditions
Varicose Veins
Interventions
DRUG

Varithena®

Varithena® (polidocanol injectable foam) 1%

DEVICE

FDA-approved Endothermal Ablation (ETA) systems

FDA-approved ETA systems, including Radiofrequency ablation (RFA) systems or Endovenous laser ablation (EVLA) systems.

Trial Locations (9)

10032

Columbia University Medical Center, New York

11794

Stony Brook University Hospital, Stony Brook

20057

Medstar Georgetown University Hospital, Washington D.C.

70360

Cardiovascular Institute of the South, Houma

77030

UT Physicians Cardiothoracic and Vascular Surgery, Houston

98004

Lake Washington Vascular, Bellevue

06820

Vascular Care Connecticut, Darien

04106

Vein Healthcare Center, South Portland

07631

Englewood Hospital and Medical Center, Englewood

Sponsors
All Listed Sponsors
lead

Boston Scientific Corporation

INDUSTRY