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.
Emergence is an important period of general anesthesia during which several problems can
occur. Coughing, hypertension, tachycardia and agitation have been observed during emergence
of general anesthesia.
Desflurane is a newer volatile agent allowing early recovery from anesthesia. This agent has
led to earlier discharge and more rapid resumption of normal activities after surgery.
However, an incidence of coughing around 70% has been reported after a desflurane-based
anesthesia. Different techniques and drugs have been studied to reduce coughing during
emergence.
Among others, the role of lidocaine given intravenously, topically, or intracuff has been
studied. The use of intracuff alkalinized lidocaine has been proven effective to reduce the
incidence of coughing during emergence of anesthesia.
Furthermore, there is some evidence supporting the administration of intravenous opioids
prior to emergence of general anesthesia to reduce perioperative coughing, agitation and
hemodynamic stimulation. However, depending on the type of opioids given, this may delay the
emergence from anesthesia. The effect of a remifentanil infusion given in combination with
isoflurane as the volatile agent has been shown to reduce the incidence of perioperative
coughing without delaying the emergence of anesthesia. Bolus doses of remifentanil have also
been proven effective to reduce the hemodynamic response to extubation.
The effect of these two modalities (alkalinized lidocaine and remifentanil) have never been
compared. This study will assess their efficacy to prevent perioperative coughing after a
desflurane-based anesthesia.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT04580030 -
Tricuapid Annular Plane Sistolic Excursion Before General Anesthesia Can Predict Hypotension After Induction
|
||
Active, not recruiting |
NCT04279054 -
Decreased Neuraxial Morphine After Cesarean Delivery
|
Early Phase 1 | |
Completed |
NCT03640442 -
Modified Ramped Position for Intubation of Obese Females.
|
N/A | |
Recruiting |
NCT04099693 -
A Prospective Randomized Study of General Anesthesia Versus Anesthetist Administered Sedation for ERCP
|
||
Terminated |
NCT02481999 -
Pre- and Postoperative EEG-Monitoring for Children Aged From 0,5 to 8 Years
|
||
Completed |
NCT04235894 -
An Observer Rating Scale of Facial Expression Can Predict Dreaming in Propofol Anesthesia
|
||
Recruiting |
NCT05525104 -
The Effect of DSA on Recovery of Anaesthesia in Children (Het Effect Van DSA op Het Herstel na Anesthesie Bij Kinderen).
|
N/A | |
Recruiting |
NCT05024084 -
Desflurane and Sevoflurane Minimal Flow Anesthesia on Recovery and Anesthetic Depth
|
Phase 4 | |
Completed |
NCT04204785 -
Noise in the OR at Induction: Patient and Anesthesiologists Perceptions
|
N/A | |
Completed |
NCT03277872 -
NoL, HR and MABP Responses to Tracheal Intubation Performed With MAC Blade Versus Glidescope
|
N/A | |
Terminated |
NCT03940651 -
Cardiac and Renal Biomarkers in Arthroplasty Surgery
|
Phase 4 | |
Terminated |
NCT02529696 -
Measuring Sedation in the Intensive Care Unit Using Wireless Accelerometers
|
||
Completed |
NCT05346588 -
THRIVE Feasibility Trial
|
Phase 3 | |
Terminated |
NCT03704285 -
Development of pk/pd Model of Propofol in Patients With Severe Burns
|
||
Recruiting |
NCT05259787 -
EP Intravenous Anesthesia in Hysteroscopy
|
Phase 4 | |
Completed |
NCT02894996 -
Does the Response to a Mini-fluid Challenge of 3ml/kg in 2 Minutes Predict Fluid Responsiveness for Pediatric Patient?
|
N/A | |
Completed |
NCT05386082 -
Anesthesia Core Quality Metrics Consensus Delphi Study
|
||
Terminated |
NCT03567928 -
Laryngeal Mask in Upper Gastrointestinal Procedures
|
N/A | |
Recruiting |
NCT06074471 -
Motor Sparing Supraclavicular Block
|
N/A | |
Completed |
NCT04163848 -
CARbon Impact of aNesthesic Gas
|