Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Ms Natalia Olejniczak
+44 (0)20 7594 0995
presize@imperial.ac.uk


Dr Katerina Spranger
+44 (0)20 3108 7553
contact@oxfordheartbeat.com


Study Location:

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Be Part of Research - Trial Details - Real-world performance evaluation of PreSize Neurovascular medical software in a clinical setting

Real-world performance evaluation of PreSize Neurovascular medical software in a clinical setting

Not Recruiting

Open to: All Genders

Age: Adult

Medical Conditions

Intracranial aneurysm


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Stenting is a common treatment for cardiovascular (heart) diseases, such as aneurysms. Stents are small spring-like metallic structures used to strengthen weak blood vessels or open them up when they become clogged. The shape and size of each blood vessel is different so there are many different stents for the doctor to choose from.
The success of the stenting procedure depends on the right fit of the stent in the affected blood vessel. Currently, it is difficult for doctors to predict which stent will give a good fit from looking at the standard brain scans. A company called Oxford Heartbeat has built a computer software (a computer program) called PreSize Neurovascular that can be used by doctors to plan the procedure and help them choose the ‘best fit’ stent for each patient by creating an accurate 3D image of their blood vessels in the brain.
PreSize Neurovascular software has demonstrated high accuracy in calculating the size of the required stent based on patients’ brain scans.
This study tries to understand the benefits of this computer program when used by doctors to help them plan for brain stenting surgeries and how well it works in real-world clinical practice.
Oxford Heartbeat will work with hospitals in England and Scotland to collect this information over a period of about 16 months from approximately 100 patients.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

01 May 2022 31 Jul 2024

In this study, the patient will not be asked to do anything that is not already part of their usual treatment. The doctor will plan the stenting procedure using their standard method, and then by using the PreSize Neurovascular computer program. The program will prepare a computer model of the patient’s blood vessels in the brain based on the scans done in preparation for the procedure. The doctor will practice fitting different stents on the computer model. Once both planning methods are complete your doctor will decide at their own discretion which stent to use based on either the standard method or the computer program method. After the procedure, the patient will continue to receive the usual treatment as prescribed by the doctor. If the patient agrees to participate, the study doctor and nurses will collect information about their medical care for study analysis, but no information that could identify the patient (e.g., name, NHS number).


Patients aged 18 years and above who are scheduled to receive treatment for an intracranial aneurysm with one of the flow diverters compatible with PreSize Neurovascular at one of the participating NHS sites.

You can take part if:



You may not be able to take part if:


1. Any reasons in the opinion of the investigator, e.g. patient cases previously fitted with coiling in the same aneurysmal area might be deemed inappropriate for the purposes of this study if it significantly impacts the contrast in the pre-operative X-ray imaging2. Unable to give informed consent


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Queens Hospital
    Rom Valley Way
    Romford
    RM7 0AG
  • Queen Elizabeth University Hospital
    1345 Govan Road
    Glasgow
    G51 4TF
  • Leeds General Infirmary
    Great George Street
    Leeds
    LS1 3EX
  • Royal Preston Hospital
    Sharoe Green Lane North Fulwood
    Preston
    PR2 9HT
  • National Hospital for Neurology & Neurosurgery
    Queen Square
    London
    WC1N 3BG
  • Royal Infirmary of Edinburgh
    51 Little France Crescent Old Dalkeith Road Edinburgh
    Lothian
    EH16 4SA
  • Cardiff & Vale University Health Board
    Heath Park
    Cardiff
    CF14 4XW
  • St Georges
    St. Georges Hospital 117 Suttons Lane
    Hornchurch
    RM12 6RS
  • The Walton Centre
    Lower Lane Fazakerley
    Liverpool
    L9 7LJ

Patients may not benefit directly from participating in this study. With the help of this study, however, the aim is to gain further insights into how future patient outcomes could be improved and NHS costs reduced through the use of the computer software.


The study is sponsored by Oxford Heartbeat Ltd and funded by National Institute for Health Research.




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Read full details for Trial ID: ISRCTN17947655

Or CPMS 50137

Last updated 06 September 2024

This page is to help you find out about a research study and if you may be able to take part

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