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EVLA and Optimal Timing of Sclerotherapy — FinnTrunk  

Venous Reflux Clinical Trial

Official title:
FinnTrunk, EVLA and Optimal Timing of Sclerotherapy

Clinical Trial Summary

The aim of the study is to investigate the optimal timing of sclerotherapy for treatment of varicose tributaries on EVLA (endogenous laser ablation) patients.

Clinical Trial Description

The study inclusion criteria is patients with main trunk (VSM, SSV, AASV) reflux to be treated with EVLA, suffering C2-C3 varicose disease, age 18-years and no severe co-morbidities. Patients with written consent will be randomized to two primary treatments groups; EVLA only and EVLA combined with sclerotherapy of varicose tributaries. The primary outcome is the requirement additional sclerotherapy on 3 month control visit. Other study outcomes are pain, quality of life (veins questionnaire), severity score and also recurring of varicose disease at 1, 3 and 5 years. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04774939
Study type Interventional
Source Turku University Hospital
Contact Harri Hakovirta, Professor
Phone +358405918811
Email haheha@utu.fi
Status Not yet recruiting
Phase N/A
Start date March 15, 2021
Completion date March 15, 2030
View Details
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