“Improving vascular health for the public benefit”
Join forces with ESVS members, including surgeons, medical manufacturers, and authorities, to reach the ultimate goal of improving patient outcomes and advancing treatment for venous diseases.
WHAT IS EVeR?
The registry is like a notebook where doctors record each patient’s diagnosis, treatment, any medical devices used, and outcomes. Pseudonymised data from it can then help doctors, researchers, and medical companies compare treatments and devices to assess effectiveness.
A project from
The European Society for Vascular Surgery (ESVS)
A non-profit organisation of over 3,000 vascular surgeons and specialists from Europe and beyond. Its goals focus on training, education, and advancing science in vascular care. ESVS operates as an independent, European platform with expertise from renowned venous specialists.
Our Mission is to enhance patient lives by improving deep venous disease treatments
The registry helps us to gather and coordinate data on vascular health, which can inform research, care and new treatments.
How can you get involved?
Your doctor may ask to include your health data in the registry. You will be given all the necessary information you need to make a decision, including details on how your information will be used. Fuller details and contacts for information are available at the bottom of the page
How does your data help?
Your data helps us build the registry, which helps patients in three main ways:
Improve outcomes for patients
Help other patients benefit from improved treatments and the identification of trends in medical practice.
Improve care quality and how it is monitored
Assist healthcare providers, researchers, and manufacturers in monitoring and enhancing the quality of care delivered.
Build the evidence base for change
Tackle existing challenge due to the lack of robust data on deep venous diseases.
This podcast, featuring Prof. Robert Hinchliffe and Prof. Stephen Black, provides additional insights into the EVeR registry.
More details
Check our Privacy notice for patient document to know who has access to your data, how are your data secured, etc.
See also the Patient information sheet which explains the study’s purpose, potential risks and benefits, confidentiality measures, and the patient’s rights, including the option to withdraw at any time.
More questions? Do not hesitate to contact our team.
- For Data Privacy questions or to exercise your rights
- General questions about the Registry
