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Effect of VarIthena on Wound Healing in Venous Leg Ulcers (VLU) — VIEW-VLU  

Venous Leg Ulcer Clinical Trial

Official title:
Observational Study of the Effect of VarIthena® on Wound Healing in the Treatment of Venous Leg Ulcers Resulting From Chronic Venous Insufficiency

Clinical Trial Summary

A 12 month, multicenter, open-label registry to observe chronic venous insufficiency resulting in VLU treated with Varithena.

Clinical Trial Description

This 12 month, multicenter, open-label registry is designed to collect treatment and outcome data related to participants treated with Varithena for great saphenous vein (GSV) system and/or anterior accessory saphenous vein (AASV) incompetence resulting in VLU. Participant are treated per Investigator's Standard of Care (SoC) and in accordance with the Full Prescribing Information (FPI) and Instructions for Use (IFU). For participants with healed ulcers during the 12 month follow-up period, VLU recurrence information is collected. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03257254
Study type Observational [Patient Registry]
Source Boston Scientific Corporation
Contact
Status Completed
Phase
Start date September 29, 2017
Completion date September 28, 2020
View Details
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