Brain surgery fluid strategy tested in 32 patients
NCT ID NCT07174128
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two different fluid management approaches during brain tumor removal surgery. 32 adults were monitored to see which method led to better recovery, measured by blood lactate levels. The goal was to find the best way to give fluids during surgery to improve patient outcomes.
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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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32 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Feb 2026
- 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.
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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: * Age above 18 years old. * Both sexes. * Patients scheduled for supra-tentorial brain tumor excision. Exclusion Criteria: * Arrhythmias. * Pulmonary hypertension. * Impaired cardiac contractility. * Impaired liver or kidney function. * Low lung compliance. * Body mass index above 40. * Intra-operative hemodynamic instability on vasopressors or inotropes. * Peripheral arterial occlusive diseases. * Hand injuries or burns that preclude the application of the Masimo device probe.
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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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Cairo University
Cairo, 12613, Egypt
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Other studies related to the condition(s) this trial covers.
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