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Clinical Trial Summary

This study aims to describe conservative and invasive treatments for patients with chronic venous disease (CVD) in Belgium, and their association with clinical and patient-reported outcomes during a follow-up of 24 months.


Clinical Trial Description

This study is an observational, prospective, multicentre study to assess the effectiveness of conservative and invasive treatments in patients with CVD in Belgium. The inclusion period of the study will last 6 months. Patients will be followed until 2 years after inclusion into the study. During the inclusion period, after confirmation of eligibility, patients with CVD diagnosed by the General Practitioner (GP) and requiring a treatment will be invited to participate in the study. About 140 GPs across Belgium will be included in the study. During the first visit, a treatment strategy will be proposed to the patient by the GP. The treatment can be conservative or invasive, depending on the severity of the disease. Patients awaiting invasive treatment may receive conservative treatment to alleviate symptoms. The choice of treatment modality is left to the discretion of the treating physician, in agreement with the patient and according to local policies. As this is an observational study, there will be no interference in the choice of treatment, and no restrictions will be imposed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06318988
Study type Observational
Source Universitaire Ziekenhuizen KU Leuven
Contact Sarah THOMIS, PhD
Phone +32498296629
Email sarah.thomis@uzleuven.be
Status Not yet recruiting
Phase
Start date May 1, 2024
Completion date May 1, 2027

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