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TACOYAKI study

Randomized controlled trials between groups with and without pharyngeal laryngeal anesthesia to examine the tolerability of bronchoscopy without pharyngeal laryngeal anesthesia - Randomized controlled trials between groups with and without pharyngeal laryngeal anesthesia to examine the tolerability of bronchoscopy without pharyngeal laryngeal anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000046975
Enrollment
200
Registered
2022-02-25
Start date
2022-03-07
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

Lung disease

Interventions

Lidocaine spray 8%, 15 times spray (about 120 mg) is not administered.Bronchoscopy day (only 1 day) Lidocaine spray 8%, 15 times spray (about 120 mg) is administered. Bronchoscopy day (only 1 day).

Sponsors

Izumi city general hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients aged 20 years or older at the time of obtaining consent (regardless of gender) 2) Research subjects who have obtained sufficient written consent to participate in this research and then voluntarily consent to the document.

Exclusion criteria

Exclusion criteria: 1) Patients with a history of hypersensitivity to lidocaine or amide-type local anesthetics 2) Patients with a history of hypersensitivity to both midazolam and propofol 3) Patients with a history of hypersensitivity to fentanyl 4) Patients with pneumothorax 5) Pregnant / lactating patients 6) In addition, patients who are judged by the principal investigator to be inappropriate as research subjects

Design outcomes

Primary

MeasureTime frame
Scale evaluation of procedure satisfaction at the time of examination judged by bronchoscopist

Secondary

MeasureTime frame
1)Scale evaluation of patient's cough at the time of examination as judged by the bronchoscopist 2) Scale evaluation of cough at the time of own examination judged by the patient 2 hours after bronchoscopy 3) Scale evaluation of discomfort at the time of own examination judged by the patient 2 hours after bronchoscopy 4) Scale evaluation of pain at the time of own examination judged by the patient 2 hours after bronchoscopy 5) Bronchoscopy time 6) Total dose of lidocaine 7) Total dose of midazolam 8) Total dose of fentanyl 9) Total dose of propofol

Countries

Japan

Contacts

Public ContactTakahiro Ueda

Izumi city general hospital Respiratory medicine

mhe.msjh.kmu@gmail.com0725411331

Outcome results

None listed

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