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Completed NCT06581731

Comparison of Remifentanil With a Combination of Remimazolam and Dexmedetomidine for Awake Tracheal Intubation

Conditions: Difficult or Failed Intubation, Sedative Adverse Reaction

Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Phase: NA
Enrollment: 64
Sponsor: Nanjing First Hospital, Nanjing Medical University

Location: Nanjing First Hospital Nanjing Jiangsu

Summary

Awake fiberoptic intubation (AFOI) requires airway surface anesthesia to inhibit pharyngeal reflex, glottis closure reflex, and cough reflex. Additionally, the use of sedative drugs can enhance patient comfort and tolerance, reduce anxiety, and eliminate harmful effects on systemic hemodynamics.The objective of this study is to compare the safety and efficacy of remifentanil alone versus a combination of dexmedetomidine and remifentanil for sedation during conscious tracheal intubation.

Eligibility Criteria

Inclusion Criteria: 1. Patients scheduled for elective open cervical spine surgery. 2. Age 18-65 years old 3. ASA classifications of I-III 4. BMI\

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06581731). StuddyBuddy aggregates publicly available trial information.