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Clinical Trials/NCT01444703
NCT01444703
Completed
Not Applicable

Randomized, Double-blind Comparison of Licorice Versus Sugar-water Gargle for Prevention of Postoperative Sore Throat and Postextubation Coughing

The Cleveland Clinic1 site in 1 country236 target enrollmentOctober 2010
ConditionsSore Throat

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sore Throat
Sponsor
The Cleveland Clinic
Enrollment
236
Locations
1
Primary Endpoint
sore throat in rest after intubation
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The investigators propose to test the hypothesis that pre-operative gargling with licorice reduces the incidence of sore throat in rest after intubation with double-lumen endotracheal tubes compared to placebo after surgery through the first four post-extubation hours.

Detailed Description

Patients will be premedicated with up to 7.5 mg p.o. midazolam, per routine. They will be told that the study involves two different solutions for prevention of post-extubation sore throat. Patients will be randomly assigned to gargle 5 minutes before induction of general anesthesia with: 1) licorice (0.5 g); or, 2) sugar (5 g). Randomization will be based on a computer-generated table of random numbers. Licorice or sugar (placebo) will be diluted in 30 ml water and filled in a small bottle by an independent apothecary of our university. All bottles will look similar and will not be opened until just before use. Investigator and patient will be blinded to the preparation used for gargle. Patients will be asked to gargle for two minutes, but not to swallow the solution. General anesthesia will be induced with fentanyl ≈3 µg/kg, propofol ≈1.5 mg/kg, and rocuronium ≈0.6 mg/kg. Complete muscle relaxation will be confirmed by absence of palpable twitches in response to supra-maximal train-of-four stimulation of the ulnar nerve at the wrist. The trachea will then be intubated as gentle as possible. Intubation will be attempted with a Macintosh laryngoscope, but the anesthesiologists may subsequently use any other intubation equipment as necessary. Initial tube size will be 37 cm left in women and 39 cm left for men; however, other sizes can be used if clinically necessary. Endotracheal tube cuffs will be inflated with air to 20-25 mmHg as necessary to maintain an adequate seal. General anesthesia will be primarily be maintained with sevoflurane. Patients lungs will be ventilated with O2 in air, usually with an inspired oxygen fraction (FiO2) of ≈40%. However, additional oxygen will be provided as clinically necessary, especially during one-lung ventilation. End-tidal CO2 will be maintained between 32 and 35 mmHg as clinically practical. Deep of anesthesia will be monitored by using bispectral index BIS, kept between 40 and 50. Small amounts of opioid will be permitted during surgery and in preparation for extubation. At the end of surgery, an intercostal plexus block -using up to 20 ml Ropivacaine 0.1% - will be performed by the surgeons. 1000 mg paracetamol will be given intravenously ten minutes before end of surgery. Post operative pain will be treated with fractional piritramid (Dipidolor) 3 mg IV as required.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
June 2011
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

d sessler

Chairman, Outcomes Research Consortium

Outcomes Research Consortium

Eligibility Criteria

Inclusion Criteria

  • Thoracic surgery with anticipated use of a double-lumen endotracheal tube;
  • Anticipated extubation in the operating room;
  • ASA Physical Status 1-3;
  • Age 18- 90

Exclusion Criteria

  • Tracheal pathology, including tracheostomy;
  • Surgery within the previous four weeks;
  • Upper-respiratory tract infection;
  • BMI higher exceeding 40 kg/m2;
  • Known or suspected allergy to licorice;
  • Use of non-steroidal anti-inflammatory drug medication within 24 hours;
  • Chronic opioid use;
  • Preoperative pain ≥ 2 on an 11-point Likert scale (0 = no pain; 10 = worst pain);
  • Known or suspected difficult airway.

Outcomes

Primary Outcomes

sore throat in rest after intubation

Time Frame: up to 4 hours post-extubation

We propose to test the hypothesis that pre-operative gargling with licorice reduces the incidence of sore throat in rest after intubation with double-lumen endotracheal tubes compared to placebo after surgery through the first four post-extubation hours.

Secondary Outcomes

  • amount of coughing(24 hours post operative)
  • sore throat in rest(first 24 hours after surgrey)
  • incidence of sore throat during swallowing(first 24 hours after surgery)
  • post-extubation coughing(up to four hours post-extubation)

Study Sites (1)

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