Trachospray Device for Airway Anesthesia

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON19975

Enrollment

Registered

2019-11-26

Start date

2019-12-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

None listed

Interventions

Subjects will be asked to inhale 4 ml lidocaine 4% via the Trachospray device

Eligibility

Inclusion criteria

Inclusion criteria: - Age between 18-60 years - ASA physical status 1

Exclusion criteria

Exclusion criteria: - Inability to cooperate with adequate airway assessment, - History of hepatic, renal and coagulation diseases, - Respiratory tract pathology - Pregnancy - Risk of regurgitation or aspiration - Allergy to amide type of local anesthetics - No written informed consent by subject

Design outcomes

Primary

Measure	Time frame
Complete anesthesia of the airway as evaluated and demonstrated by awake laryngobronchoscopy with minimal discomfort for the subject.	—

Contacts

Public ContactG.J. van Geffen

Radboudumc

Geert-Jan.vanGeffen@radboudumc.nl+3124 365 57 55

Outcome results