Anesthesia Clinical Trial
Official title:
Efficacy of Alkalinized Lidocaine in the Endotracheal Tube Cuff Compared to a Bolus Dose of Intravenous Remifentanil on the Incidence of Coughing During Emergence of Anesthesia
This study is designed to compare the effects of alkalinized lidocaine in the endotracheal
tube cuff to a bolus dose of remifentanil given prior to the emergence of anesthesia:
- on the incidence of perioperative coughing
- on the time needed for the emergence of a desflurane-based anesthesia
- on the incidence of sore throat after extubation.
The investigators hypothesis is that the use of alkalinized lidocaine in the endotracheal
tube cuff will reduce the incidence of perioperative coughing after a desflurane-based
anesthesia.
Status | Completed |
Enrollment | 85 |
Est. completion date | October 2012 |
Est. primary completion date | October 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Patients aged 18-80 years - Physical status 1-3 - Patients undergoing elective surgery under general anesthesia requiring oral endotracheal intubation (excluding head and neck surgery) - Expected duration of surgery of at least 1.5 hour. Exclusion Criteria: - Current use of ACE inhibitor - Chronic cough - Asthma or severe pulmonary disease - Pulmonary tract infection - Anticipated difficult intubation - Current use of opioids - Current use of cough medicine - Contraindication to remifentanil, lidocaine - Pregnancy - Symptomatic cardiac, renal or hepatic disease |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Canada | Centre Hospitalier de l'Université de Montréal | Montreal | Quebec |
Lead Sponsor | Collaborator |
---|---|
Centre hospitalier de l'Université de Montréal (CHUM) | Centre de Recherche du Centre Hospitalier de l'Université de Montréal |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of coughing during emergence and after extubation | From emergence until 10 minutes after extubation | Yes | |
Secondary | Time to emergence | From the discontinuation of Desflurane until extubation | Yes | |
Secondary | Incidence of sore throat one hour after extubation | Assessed one hour after extubation | Yes |
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