Common ICU procedure may briefly raise brain pressure — study investigates the risk
NCT ID NCT07704528
First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time
Summary
This observational study looks at how inserting a central venous catheter into the neck affects pressure inside the skull in patients with acute brain injury. Researchers will monitor brain pressure, blood flow, and oxygen levels during and after the procedure in about 120 ICU patients. The goal is to understand the size and duration of any pressure changes, which could help make this routine procedure safer for brain-injured patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors understand the risks of a common ICU procedure and guide safer care for patients with acute brain injury.
- What could go wrong
- This is an observational study, not a treatment trial, so it will not directly improve outcomes. Results may not apply to all brain injury patients or hospital 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.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Dec 2029
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.
Who is studied
Adult patients (≥18 years) with acute brain injury (including traumatic brain injury, spontaneous intracerebral hemorrhage, large hemispheric infarction, and aneurysmal subarachnoid hemorrhage) who require invasive intracranial pressure monitoring and are scheduled for clinically indicated percutaneous internal jugular vein catheterization. Patients with ICP \>22 mmHg within 48 hours prior to the procedure, contraindications to jugular catheterization (e.g., severe coagulopathy, local neck pathology, bilateral catheters already in place), or who are pregnant/breastfeeding are excluded. The study population is recruited from two ICUs in China (Beijing Tiantan Hospital and Guiyang Second People's Hospital).
- 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: * Age ≥ 18 years * Admitted to the ICU with acute brain injury (including traumatic brain injury, spontaneous intracerebral hemorrhage, large hemispheric infarction, or aneurysmal subarachnoid hemorrhage) and ICU stay ≥ 24 hours * Invasive intracranial pressure (ICP) monitoring in place as part of clinical care * Scheduled to undergo percutaneous internal jugular vein catheterization (central venous catheter) as determined by the treating physician * Written informed consent obtained from the patient or legally authorized representative Exclusion Criteria: * Informed consent not obtained * Intracranial pressure (ICP) \> 22 mmHg within the past 48 hours * Any contraindication to internal jugular catheterization exists (severe coagulopathy with INR \> 1.5 or platelets \< 50×10⁹/L; neck infection, tumor, prior surgery or anatomical abnormality on either side; or bilateral jugular veins already catheterized) * Pregnancy or breastfeeding
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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.
Contacts and locations
Locations
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Beijing Tiantan Hospital, Capital Medical University
Beijing, Beijing Municipality, 100070, China
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The Second People's Hospital of Guiyang
Guiyang, Guizhou, 550081, China
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Other studies related to the condition(s) this trial covers.
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