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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
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01489683
Enrollment
50
Registered
2011-12-12
Start date
2011-05-31
Completion date
2012-05-31
Last updated
2012-07-16

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

Conditions

Drug Usage

Keywords

intubating conditions, propofol, remifentanil, topical lidocaine

Brief 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.

Interventions

DRUGlidocaine

3 ml of 4% lidocaine was instilled to larynx and trachea

DRUGnormal saline

3 ml of normal saline was instilled to larynx and trachea before endotracheal intubation

Sponsors

Ajou University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* ASA I, II patients undergoing general anesthesia for reduction of nasal bone fracture

Exclusion criteria

* bronchial asthma, * COPD, * hypertension, * anticipated difficult airway

Design outcomes

Primary

MeasureTime frameDescription
Overall acceptable conditions for tracheal intubationbaseline from 5 min of TCI was maintainedFour minutes after start of propofol-remifentanil TCI, 3 ml of normal saline or 3 ml of 4% lidocaine was instilled to larynx and trachea, and one minute later, intubation was performed in double-blinded fashion.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026