Can a smart app make brain aneurysm Follow-Up better?
NCT ID NCT07569562
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a digital platform called GetReady that helps doctors and patients track brain aneurysm follow-up data, including symptoms and quality of life. About 200 people with brain aneurysms will use the platform during routine care. The goal is to see if it improves health-related quality of life and makes follow-up more efficient.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- GetReady digital platform (a CE-marked digital tool for collecting and visualizing clinical, radiological, and patient-reported data during routine follow-up)
- What this could lead to
- If it works, this could show that a simple digital tool helps doctors and patients manage brain aneurysm follow-up more effectively, potentially improving quality of life.
- What could go wrong
- This is an early implementation study, not a treatment trial. It may not show clear benefits, and results might not apply to all patients or settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of cerebral aneurysm * Access to one of the following: compatible mobile phone, computer, or tablet with internet access * Sufficient internet connection for use of the digital platform * When the patient cannot or does not wish to use the application directly, participation may occur through a designated caregiver or family member, after informed consent Exclusion Criteria: * Patients treated with surgical clipping * Absence of informed consent
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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