New study tests Needle-Free blood pressure monitoring during brain surgery
NCT ID NCT07246148
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares a non-invasive continuous blood pressure monitor (ClearSight) to the standard arterial catheter in 50 adults undergoing coil embolization for unruptured brain aneurysms. The goal is to see if the non-invasive method can safely detect blood pressure changes and reduce the need for invasive catheters. Participants are randomly assigned to one of the two monitoring methods during their procedure.
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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 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Aug 2027
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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19 to 80 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients (≥19 and ≤80 years old) scheduled for elective coil embolization of unruptured intracranial aneurysms under general anesthesia. * American Society of Anesthesiologists (ASA) physical status classification I-III. Exclusion Criteria: * Patients who do not provide informed consent. * Patients unable to understand or follow study instructions due to physical or mental limitations. * Patients in whom radial arterial catheterization is not feasible (e.g., peripheral vascular disease, skin disorders at the insertion site, absence of radial/ulnar artery, or orthopedic conditions of the upper extremity). * Patients with peripheral vascular circulatory disorders. * Patients with morbid obesity (BMI ≥ 40 kg/m²) \[Eley et al., 2021\]. * Patients who are hemodynamically unstable preoperatively or expected to be unstable during the perioperative period.
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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 places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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Korea University Anam Hospital
RECRUITINGSeoul, 02841, South Korea
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- A simple ultrasound might replace invasive pressure monitoring
- Can a tiny mesh device defuse brain aneurysms? a registry investigates