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Starting soon Not applicable

Remifentanil vs Esmolol During Intubation for Cerebral Aneurysm Coil Embolization

NCT07660861 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-22
Last updated
2026-06-22

Condition(s) studied

Cerebral Aneurysm UnrupturedIntracranial Pressure

Investigational drug(s) / intervention(s)

Remifentanil →Esmolol →

Remifentanil: Remifentanil 0.5-1 µg/kg IV administered over 90 seconds before endotracheal intubation.

Esmolol: Esmolol 0.5-1 mg/kg IV administered over 90 seconds before endotracheal intubation.

Study summary

Endotracheal intubation may cause significant increases in blood pressure, heart rate, and intracranial pressure, particularly in patients undergoing cerebral aneurysm coil embolization. Remifentanil and esmolol are commonly used agents to attenuate these responses during anesthesia induction.

This randomized controlled trial aims to compare the effects of remifentanil and esmolol administered before endotracheal intubation on optic nerve sheath diameter/eyeball transverse diameter ratio (ONSD/ETD), a noninvasive surrogate marker of intracranial pressure, as well as hemodynamic responses in patients undergoing elective cerebral aneurysm coil embolization.

The findings may help identify the most effective strategy for minimizing intubation-related intracranial pressure changes and hemodynamic fluctuations in neurointerventional anesthesia practice.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * American Society of Anesthesiologists (ASA) physical status I-III * Scheduled for elective cerebral aneurysm coil embolization under general anesthesia * Planned endotracheal intubation * Ability to provide written informed consent Exclusion Criteria: * Emergency procedures * Hemodynamic instability before induction of anesthesia * Severe cardiac conduction abnormalities or clinically significant arrhythmias * Contraindication or allergy to remifentanil or esmolol * Chronic opioid use or opioid dependence * Known orbital disease, ocular trauma, or conditions interfering with optic nerve sheath diameter measurements * Anticipated difficult airway * Pregnancy * Refusal to participate in the study

Primary outcome measure(s)

  • Change in ONSD/ETD Ratio at 5 Minutes After Endotracheal Intubation — 5 minutes after endotracheal intubation
    Difference between baseline (pre-intubation) and 5-minute post-intubation optic nerve sheath diameter-to-eyeball transverse diameter ratio (ONSD/ETD).

Trial sites (1)

FacilityCityRegionStatus
Fatih Sultan Mehmet Training and Research Hospital Istanbul Istanbul
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07660861 on ClinicalTrials.gov ↗ ← All trials in Turkey