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The effect-site concentration of remifentanil for maintaining hemodynamic stability during double-lumen tube intubation and fiberoptic bronchoscopy under remimazolam-based general anesthesia: a prospective dose-finding study

The effect-site concentration of remifentanil for maintaining hemodynamic stability during double-lumen tube intubation and fiberoptic bronchoscopy under remimazolam-based general anesthesia: a prospective dose-finding study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011748
Enrollment
40
Registered
2026-03-19
Start date
2026-03-27
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : This study investigates the optimal effect-site concentration (Ce) of remifentanil required to maintain hemodynamic stability during double-lumen tube (DLT) intubation and fiberoptic bronchosco

Sponsors

Samsung Changwon Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients aged 19 to 64 years. Patients scheduled for elective surgery requiring general anesthesia with double-lumen tube intubation and fiberoptic bronchoscopy. Patients with an American Society of Anesthesiologists (ASA) physical status of I ~III Patients who have provided voluntary written informed consent after receiving a detailed explanation of the study.

Exclusion criteria

Exclusion criteria: Patients with an anticipated difficult intubation. Patients with psychiatric disorders resulting in impaired decision-making or communication skills. Patients with cognitive impairment. Patients with heart failure or a history of myocardial infarction within the past 6 months. Patients with severe arrhythmia. Patients with severe pulmonary disease. Patients with a history of hypersensitivity to remimazolam or remifentanil. Pregnant or lactating women. Any other patients deemed inappropriate for study participation by the investigator.

Design outcomes

Primary

MeasureTime frame
Maintenance of hemodynamic stability during double-lumen tube (DLT) intubation and fiberoptic bronchoscopy

Secondary

MeasureTime frame
Changes in mean arterial pressure (MAP) and heart rate (HR);Incidence of hemodynamic adverse events (ehypotension, bradycardia, hypertension, tachycardia) and the use of rescue medications (ephedrine, atropine, nicardipine, esmolol, phenyleprine);Incidence and severity score of cough and somatic movement during intubation and bronchoscopy manipulation

Countries

Korea, Republic of

Contacts

Public ContactSungae Cho

Samsung Changwon Medical Center

sachosa@naver.com+82-55-233-6045

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Apr 3, 2026