NCT06776900 Fiberoptic Intubation in Lateral Versus Supine Position in Pediatrics Undergoing Non-head-and-neck Surgery
| NCT ID | NCT06776900 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cairo University |
| Condition | Video-assisted |
| Study Type | INTERVENTIONAL |
| Enrollment | 50 participants |
| Start Date | 2025-01-18 |
| Primary Completion | 2025-07 |
Eligibility & Interventions
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 50 participants in total. It began in 2025-01-18 with a primary completion date of 2025-07.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Fiberoptic intubation was first described in the late 1960s and has since become an effective and well-established technique for airway management in awake, sedated, and anesthetized patients. This technique is especially useful in patients with known or suspected difficult airways such as those with limited mouth opening, reduced neck mobility, cervical spine injury, obesity, or an elevated risk for aspiration. The benefits of fiberoptic intubation also include fewer complications such as tooth injury and oropharyngeal bleeding; and the opportunity for optimal positioning of double-lumen tubes in patients undergoing thoracic surgery. Anesthesiologists may be confronted with situations in which patients in a lateral position during surgery experience an accidental loss of airway patency. Intubation with direct laryngoscopy is more challenging and time-consuming in patients in the lateral position than in the supine position, particularly when there is an abrupt loss of airway patency, as demonstrated by prior research. These observations suggest that there is an unmet need for a reliable method of airway management for patients in the lateral position. Although the airway is of a larger caliber and ventilation renders less peak and better oxygenation when patients are in the lateral position, glottic view was unfavorable for intubation when Macintosh direct laryngoscope was used in this position. This could be the reason why such a procedure is unfamiliar in anesthesia even when it is the most needed in special situations. Flexible fiberoptic intubation in lateral position would be convenient in emergency situations like accidental extubation during surgery or inadequate regional anesthesia requiring general anesthesia. Flexible fiberoptic intubation in lateral position would be of significant assistance in neurosurgical patients especially those with occipital lesions and patients with difficult airway scores with limited mouth opening or neck extension. After thorough literature review, we found that studies comparing flexible video-assisted fiberoptic intubation in the lateral versus supine position in pediatrics are lacking.
Eligibility Criteria
Inclusion Criteria: * Children aged 2-10 years old. * Both genders. * ASA physical status I and II. * Elective non-head-and-neck surgeries. Exclusion Criteria: * Refusal of patients. * Head and neck surgeries or with history of previous ones. * Head, neck and lung congenital deformities or pathologies. * Patients with expected difficult intubation (based on examination). * Patients with neuromuscular disorders. * Hypoxia: defined as low oxygen saturation (SpO2) ≤ 95% on room air. * Trauma patients or patients requiring emergency procedures.
Contact & Investigator
Mariam KE Mohammed, MBBCh
PRINCIPAL INVESTIGATOR
Cairo University
Frequently Asked Questions
Who can join the NCT06776900 clinical trial?
This trial is open to participants of all sexes, aged 2 Years or older, up to 10 Years, studying Video-assisted. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06776900 currently recruiting?
Yes, NCT06776900 is actively recruiting participants. Contact the research team at drknawwar@cu.edu.eg for enrollment information.
Where is the NCT06776900 trial being conducted?
This trial is being conducted at Cairo, Egypt.
Who is sponsoring the NCT06776900 clinical trial?
NCT06776900 is sponsored by Cairo University. The principal investigator is Mariam KE Mohammed, MBBCh at Cairo University. The trial plans to enroll 50 participants.