Brain protein may guide hydrocephalus treatment
NCT ID NCT05399602
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether measuring a protein called NfL in the blood or spinal fluid can help doctors manage hydrocephalus, a condition where too much fluid puts pressure on the brain. Researchers studied 41 adults with this condition to see if NfL levels relate to symptoms and treatment decisions. The goal was to learn if this test could be a useful tool, not to test a new treatment.
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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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41 people
The number who actually took part.
- Started
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Dec 2023
- Finished
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Sep 2025
- 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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50 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.
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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: * In group A: * Patients with diagnosed communicating hydrocephalus * MMSE \> 10 points * Absence of any structural laesion on MRI or CT * Accepted Informed consent * In group B: * MMSE \> 10 points * Absence of any structural laesion on MRI or CT * Accepted Informed consent * Elective spinal surgery without affecting dural sac and the spinal cord * Surgery shorter than 120 minutes of lasting the general anesthesia Exclusion Criteria: * Non-communicating hydrocephalus * Structural laesion on MRI or CT (tumour, contusion, aneurysm) * MMSE \< 10 points * Life-expectancy shorter than 1 year * Pre-existing other type of demetia (m. Alzheimer, vascular dementia) * Surgery lasting more than 120 minutes * Blood loss more than 500 ml * Opening of dural sac (liquororhea) * Adverse events during general anestesia: MAP\<60 mm Hg more than 5 minutes, arythmia with need for farmacological treatment
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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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University Hospital Hradec Kralove
Hradec Králové, 50005, Czechia
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