Brain damage markers tracked during robotic prostate surgery
NCT ID NCT05692804
First seen Jul 29, 2026 · Last updated Jul 30, 2026 · Updated 1 time
Summary
This study looks at whether the steep head-down position used during robot-assisted prostate surgery can cause subtle brain injury. Researchers measure three brain-specific proteins (S100B, GFAP, and NSE) in the blood before and after surgery, along with simple cognitive tests. The goal is to see if these markers rise, signaling possible brain stress or damage. About 59 adults undergoing robotic prostate removal will take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Measurement of S100B, GFAP, and NSE biomarkers in blood, plus cognitive tests (MMSE, MoCA)
- What this could lead to
- If brain damage markers rise during robotic prostate surgery, it could lead to safer positioning guidelines to protect patients' brains.
- What could go wrong
- This is a small, early study measuring temporary chemical changes, not actual brain injury. The markers may not reflect real harm.
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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59 people
The number who actually took part.
- Started
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Mar 2022
- Finished
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Sep 2024
- 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
Patients aged 18-75 who were operated on under general anesthesia for RALRP surgery
- Ages
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18 to 70 years
- Sex
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Male participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * All patients aged 18-75 who were operated on under general anesthesia for RALRP surgery and agreed to participate in the study will be included. Exclusion Criteria: * Participants who did not accept the study, had active intracranial pathology and history of intracranial pathology will not be included in the 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.
Contacts and locations
Locations
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Akdeniz University Hospital
Antalya, 07070, Turkey (Türkiye)
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