Clinical Trials Directory

Trials / Completed

CompletedNCT06962813

Transdermal Radiofrequency V ERASER Versus Polidocanol Sclerotherapy for Reticular Veins and Telangiectasias

Transdermal Radiofrequency (V ERASER) Versus Polidocanol Sclerotherapy for the Treatment of Reticular Veins and Telangiectasias: A Randomized Controlled Trial (TYPER Trial)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
46 (actual)
Sponsor
Science Valley Research Institute · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This study tested V Eraser, Transdermal radiofrequency versus polidocanol sclerotherapy for the treatment of reticular veins and telangiectasia of the legs

Detailed description

Chronic Venous Disease causes symptoms such as pain, edema, and skin manifestations, including telangiectasias and varicose veins. Sclerotherapy with polidocanol is the gold standard treatment; however, technologies such as laser devices and transdermal radiofrequency are also available. The V Eraser, a device that combines transdermal radiofrequency and sclerotherapy, was developed to treat these conditions. Methods: This was a prospective, randomized, and comparative study comparing V Eraser with sclerotherapy for the treatment of telangiectasias and reticular veins. Forty-one patients were randomized to either V Eraser or polidocanol sclerotherapy and underwent a single treatment session. Efficacy was assessed using the Aberdeen Varicose Vein Questionnaire and vessel clearance analysis in pre- and post-treatment images.

Conditions

Interventions

TypeNameDescription
PROCEDURERadiofrequency V Eraserstandar of care sclerotherapy

Timeline

Start date
2023-01-10
Primary completion
2025-01-02
Completion
2025-04-10
First posted
2025-05-08
Last updated
2025-05-08

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT06962813. Inclusion in this directory is not an endorsement.