Clinical Trials Directory

Trials / Completed

CompletedNCT01489683

Intubating Conditions During Propofol-remifentanil Anesthesia With Topical Lidocaine

Effect of Tracheal Lidocaine on Intubating Conditions During Propofol-remifentanil TCI Without Neuromuscular Blockade

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Ajou University School of Medicine · Academic / Other
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Not accepted

Summary

When not using neuromuscular blocking agent, even at optimal dosage, target-controlled infusion (TCI) of propofol and remifentanil occasionally produce unsatisfactory intubating conditions. Therefore, the investigators evaluated that the effect of tracheal lidocaine on the intubating conditions for tracheal intubation during anesthesia induction of propofol and remifentanil TCI without neuromuscular blocking agent in day-case anesthesia.

Detailed description

Anesthesia was induced with propofol-remifentanil TCI with the effect-site concentration of 5μg/ml and 5ng/ml, respectively. After TCI, 3 ml of normal saline or 3 ml of 4% lidocaine was instilled to larynx and trachea, following intubation was performed.

Conditions

Interventions

TypeNameDescription
DRUGlidocaine3 ml of 4% lidocaine was instilled to larynx and trachea
DRUGnormal saline3 ml of normal saline was instilled to larynx and trachea before endotracheal intubation

Timeline

Start date
2011-05-01
Primary completion
2012-04-01
Completion
2012-05-01
First posted
2011-12-12
Last updated
2012-07-16

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01489683. Inclusion in this directory is not an endorsement.