Clinical Trials Directory

Trials / Completed

CompletedNCT03856814

Market Penetration of Laser Therapy in Venous Surgery: Ziekenhuis Oost-Limburg - Ziekenhuis Maas En Kempen Center Experience

Market Penetration of Laser Therapy in Venous Surgery: ZOL - ZMK Center Experience

Status
Completed
Phase
Study type
Observational
Enrollment
500 (actual)
Sponsor
Duomed · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this registry is to evaluate the indication for EndoVenous Laser Ablation (EVLA) therapy. Can this be enhanced? What are the reasons for not using the laser? Therefore, this study aims to define clear indications for EVLA by registering the incentives of the participating investigators to use the laser instead of conventional corrective surgery for the treatment of varicose veins, at baseline and post-operative. Additionally, the efficacy and safety of the different varicose vein treatments will be evaluated by registering procedural characteristics, anatomic outcome (duplex ultrasound), quality of life (AVVQ) and postoperative pain (VAS).

Conditions

Interventions

TypeNameDescription
DEVICEELVeS® Radial® 2ring slim fiber used for EndoVenous Laser AblationDevice for endovenous laser ablation manufactured by Biolitec AG company (ELVeS system) - diode laser with a wavelength of 1470 nm

Timeline

Start date
2019-03-15
Primary completion
2023-01-13
Completion
2023-11-08
First posted
2019-02-27
Last updated
2024-09-05

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT03856814. Inclusion in this directory is not an endorsement.