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Comparison of Videolaryngoscope and Flexible Fiberscope for Tracheal Intubation under Maximal Assistance in Patients with a Cervical Collar: Randomized Controlled Non-Inferiority Trial

Comparison of Videolaryngoscope and Flexible Fiberscope for Tracheal Intubation under Maximal Assistance in Patients with a Cervical Collar: Randomized Controlled Non-Inferiority Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010708
Enrollment
262
Registered
2025-07-03
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

None listed

Interventions

Procedure/Surgery : Anesthesia induction and perioperative management will be performed identically in both groups. Tracheal intubation will be conducted by one of four board-certified anesthesiologis
failure is defined as periephral oxygen satuation 180 seconds, after which appropriate rescue is performed. In addition to first-attempt success rate, assessments include glottic view (Cormack-Lehane

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients scheduled for general anesthesia with tracheal intubation, classified as American Society of Anesthesiologists physical status I–III, and with cervical spine pathology identified in the final interpretation of preoperative cervical imaging (X-ray, computed tomography, or magnetic resonance imaging).

Exclusion criteria

Exclusion criteria: Patients who do not consent to participate in the study Patients with a high risk of pulmonary aspiration or a history of gastroesophageal reflux Patients who have not maintained appropriate preoperative fasting Patients with congenital or acquired upper airway lesions (e.g., tumors, polyps, trauma, abscess, inflammation, foreign bodies, etc.) Patients with a history of surgery or radiation therapy involving the upper airway Patients with coagulopathy or bleeding disorders Patients with severely mobile or loose teeth

Design outcomes

Primary

MeasureTime frame
First-attempt success rate of tracheal intubation

Secondary

MeasureTime frame
Tracheal intubation time;Number of intubation attempts;Rescue ventilation;Videolaryngoscopic Cormack-Lehane grade;Percentage of glottic opening (POGO) score;Blood in oral cavity;Blood staining on endotracheal tube;Gum bleeding;Teeth injury;Tongue injury;Lip injury;Hoarseness;Sore throat;Mean arterial pressure;Heart rate;Peripheral oxygen saturation;Bispectral index

Countries

Korea, Republic of

Contacts

Public ContactHyongmin Oh

Seoul National University Hospital

hyungmin0118@naver.com+82-2-2072-4908

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026