Ireland
--:--IST
Recruiting Not applicable

Effects of Sufentanil on the Intraoperative Hemodynamics

NCT06091904 · tracked via the Priya Life Science South Korea tracker
Phase
Not applicable
Started
2023-11-24
Last updated
2025-09-16

Condition(s) studied

Intraoperative Hypotension

Investigational drug(s) / intervention(s)

Sufentanil →Remifentanil →

Sufentanil: Induction: sufentanil TCI 0.3 ng/ml Maintenance: sufentanil TCI 0.05-0.5 ng/ml

Remifentanil: Induction: remifentanil TCI 3 ng/ml Maintenance: remifentanil TCI 0.5-5 ng/ml

Study summary

This study is a randomized, controlled trial. A total of 92 patients will be randomized to receive sufentanil or remifentanil during extracranial-intracranial bypass surgery.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients who undergo elective extracranial-intracranial bypass surgery * American Society of Anesthesiologists grade 1,2,3 * Age \> 18 years old Exclusion Criteria: * Refuse to participate to the study * American Society of Anesthesiologists grade 4 * Body Mass Index \< 18.5 kg/m2 or \> 35 kg/m2 * Allergic history of opioid * pregnant * MAO Inhibitor user * Severe respiratory insufficiency

Primary outcome measure(s)

  • Intraoperative hypotension — During surgery
    MAP \< 80 mmHg

Trial sites (1)

FacilityCityRegionStatus
Seoul National University Bundang Hospital Seongnam-si Gyeonggi-do Recruiting
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 NCT06091904 on ClinicalTrials.gov ↗ ← All trials in South Korea