MedPath

Effect of Lidocaine 1% and 2% in the Tube Cuff on Postoperative Sore Throat and Cough

Not Applicable
Conditions
Postoperative Cough
Postoperative Sore Throat
Interventions
Other: cuff inflation with air
Drug: cuff inflation with lidocaine 1%
Drug: cuff inflation with lidocaine 2%
Other: Induction of anesthesia
Other: Maintenance of anesthesia
Other: Endotracheal intubation
Other: Systematic post-operative analgesia
Registration Number
NCT03792776
Lead Sponsor
Ogarite Habib
Brief Summary

Comparing the effect of different methods of endotracheal tube cuff inflation on the occurrence of a postoperative sore throat and cough (Air vs Lidocaine 1% vs Lidocaine 2%).

Detailed Description

Eligible patients undergoing general anesthesia will be randomized and assigned to three groups:

Group A: Endotracheal tube cuff inflation with air Group B: Endotracheal tube cuff inflation with Lidocaine 1% Group C: Endotracheal tube cuff inflation with Lidocaine 2%

The induction of anesthesia will be made following a preoxygenation with a facial mask with 100% Oxygen. It consists on the intravenous injection of Sufentanil 5 mcg or Fentanyl 50mcg, Lidocaine 1mg/Kg, Propofol 2.5mg/kg, Rocuronium 0.6mg/kg or Cisatracurium 0.15mg/kg.

Maintenance of anesthesia will be done by sevoflurane + nitrous oxide, and reinjections of morphinomimetics and curare will be made as needed (the total doses will be noted at the end of the intervention).

The intubation is made by a N° 7.5 tube in men and a N° 7 tube in women. Cuff inflation will be done upon placement of the endotracheal tube. The cuff's pressure will be monitored at several intervals of the intervention and kept \< or = 20 centimeter of water (cmH2O).

The volume of lidocaine used will never exceed 5 mg / kg for the patient to be protected from the local toxicity of the local anesthetic in case of accidental rupture of the balloon.

All patients will receive Paracetamol every 6 hours for the first 24 hours after the end of surgery.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Patients over 18 years old
  • American Society of Anesthesiologists classification (ASA) category 1 or 2
  • High pressure, low volume endotracheal tube - (Lo-pro)
Exclusion Criteria
  • Ear nose and throat and cranial surgery
  • Ear nose and throat pathologies
  • Asthma and bronchial hyperreactivity
  • Chronic cough
  • Diabetes
  • Cognitive disorders
  • Swallowing disorders
  • Corticotherapy during the last week
  • Allergy to lidocaine
  • Urgent surgery
  • Nasogastric, oro-gastric
  • Ventral position
  • More than 2 intubation attempts
  • Continuous intravenous infusion of lidocaine intraoperatively.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Aircuff inflation with airEndotracheal tube cuff inflation with air
Lidocaine 2%Systematic post-operative analgesiaEndotracheal tube cuff inflation with Lidocaine 2%
AirInduction of anesthesiaEndotracheal tube cuff inflation with air
AirSystematic post-operative analgesiaEndotracheal tube cuff inflation with air
Lidocaine 1%cuff inflation with lidocaine 1%Endotracheal tube cuff inflation with Lidocaine 1%
Lidocaine 2%cuff inflation with lidocaine 2%Endotracheal tube cuff inflation with Lidocaine 2%
Lidocaine 2%Maintenance of anesthesiaEndotracheal tube cuff inflation with Lidocaine 2%
Lidocaine 1%Maintenance of anesthesiaEndotracheal tube cuff inflation with Lidocaine 1%
Lidocaine 1%Endotracheal intubationEndotracheal tube cuff inflation with Lidocaine 1%
Lidocaine 1%Systematic post-operative analgesiaEndotracheal tube cuff inflation with Lidocaine 1%
AirEndotracheal intubationEndotracheal tube cuff inflation with air
Lidocaine 1%Induction of anesthesiaEndotracheal tube cuff inflation with Lidocaine 1%
Lidocaine 2%Induction of anesthesiaEndotracheal tube cuff inflation with Lidocaine 2%
AirMaintenance of anesthesiaEndotracheal tube cuff inflation with air
Lidocaine 2%Endotracheal intubationEndotracheal tube cuff inflation with Lidocaine 2%
Primary Outcome Measures
NameTimeMethod
Sore throat intensity 2at 2 hours after extubation

Throat pain evaluation using the visual analog scale of pain (range from 0 cm (no pain) to 10 cm (very intense pain))

Cough intensity 2at 2 hours after extubation

Cough intensity evaluation using the visual analog scale of cough (range from 0 cm (no cough) to 10 cm (very severe cough))

Cough intensity 6at 6 hours after extubation

Cough intensity evaluation using the visual analog scale of cough (range from 0 cm (no cough) to 10 cm (very severe cough))

Cough intensity 24at 24 hours after extubation

Cough intensity evaluation using the visual analog scale of cough (range from 0 cm (no cough) to 10 cm (very severe cough))

Cough intensity 0hour 0 after extubation

Cough intensity evaluation using the visual analog scale of cough (range from 0 cm (no cough) to 10 cm (very severe cough))

Sore throat intensity 0hour 0 after extubation

Throat pain evaluation using the visual analog scale of pain (range from 0 cm (no pain) to 10 cm (very intense pain))

Sore throat intensity 24at 24 hours after extubation

Throat pain evaluation using the visual analog scale of pain (range: from 0 cm (no pain) to 10 cm (very intense pain))

Sore throat intensity 6at 6 hours after extubation

Throat pain evaluation using the visual analog scale of pain (range from 0 cm (no pain) to 10 cm (very intense pain))

Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath