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
| Type | Name | Description |
|---|---|---|
| DRUG | lidocaine | 3 ml of 4% lidocaine was instilled to larynx and trachea |
| DRUG | normal saline | 3 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.