Serum lidocaine levels following administration of topical lidocaine during in office laryngopharyngeal procedures

Not Applicable

Recruiting

• Conditions: anaesthesia; lidocaine toxicity; Anaesthesiology - Anaesthetics

• Registration Number: ACTRN12616000058471
• Lead Sponsor: Auckland District Health Board

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-01-20
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Patients undergoing awake laryngopharyngeal procedures in the office requiring topical anaesthesia
Age >18 years
Ability to give informed consent

Exclusion Criteria

Age <18 yrs
Preexisting increased risk of bleeding or thrombosis
Coagulation disorders
Renal disease
Hepatic disease
Pre-exisiting cardiac conduction abnormality
Inability to provide informed consent
Allergy to lidocaine

Study & Design

• Study Type: Observational
• Study Design: Not specified