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Study on the tolerability of fiberoptic intubation using a fine particle nebulizer

Study on the tolerability of fiberoptic intubation using a fine particle nebulizer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs042240070
Enrollment
39
Registered
2024-08-13
Start date
2024-08-13
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

none

Interventions

After spraying lidocaine with a nebulizer and confirming sleep onset with propofol, perform endotracheal intubation.

Sponsors

Tamura Takahiro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients 18 years or older who have consented to the study and who undergo surgery under general anesthesia. In the first stage, patients scheduled to undergo spinal surgery. Patients who are planning to obtain an A-line during general anesthesia.

Exclusion criteria

Exclusion criteria: Age under 18 years old Patients who are judged to be unsuitable for participation in this study by the principal investigator or co-investigator

Design outcomes

Primary

MeasureTime frame
Percentage of cases in which endotracheal intubation was achieved without additional local anesthesia using Jackson nebulizer.

Secondary

MeasureTime frame
Presence and number of reflexes (gag reflex, cough reflex) during the procedure Time from completion of inhalation to intubation Total local anesthetic usage Number of additional local anesthetic sprays/Local anesthetic amount Type and amount of additional sedatives and analgesics Rate of muscle relaxants given before intubation

Contacts

Public ContactTakahiro Kuwabara

Nagoya University School of Medicine Hospital

kuwa0525bara@gmail.com+81-52-744-2340

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026