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Study identifier: NCT06884657 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Mannitol on Propofol Level

Condition: Mannitol Adverse Reaction  ·  Sponsor: Cukurova University

PhasePhase 4
Planned participants40
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

Group 1 will include 20 patients aged 18 years and over, American Society of Anesthesiologist (ASA) II-III class, who will undergo supratentorial tumor surgery, and Group 2 will include 20 patients who will undergo pituitary surgery without mannitol. Total intravenous anesthesia (TIVA) will be adjusted to propofol 4 µg/dl and remifentanil 2-4 µg/dl with target-controlled infusion pumps. In the mannitol group, 2.5 ml/kg (0.5 g/kg) will be given to all patients 20 minutes after induction and the mannitol infusion will be adjusted to be 10 minutes.In Group 2, mannitol will not be used and 2.5 ml/kg isotonic will be administered in 10 minutes. Both blood and urine samples will take for measurement to propofol levels.

This description comes directly from the study's public registry record.

Talk to the study team

Ebru Biricik  ·  +905052420223  ·  ebrubiricik01@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Çukurova UniversityÇukurova, Adana, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT06884657