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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02968823
Other study ID # 1308/2016
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2017
Est. completion date September 30, 2022

Study information

Verified date August 2023
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our primary aim is to determine whether licorice gargling provides meaningful analgesia after oral surgery. Specifically, we propose to test the primary hypothesis that gargling with licorice solution reduces pain after oral surgery more than gargling with sugar water. Because effective analgesia can reduce pain and/or opioid consumption, we will jointly evaluate verbal response pain scores and overall morphine consumption considering licorice to be beneficial only if it proves non-inferior on both measures and superior on at least one.


Recruitment information / eligibility

Status Completed
Enrollment 127
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 12 Years to 99 Years
Eligibility Inclusion Criteria: 1. Oropharyngeal surgeries including:Panendoscopic surgery; elective tonsillectomy/adenotonsillectomy; demarcation and biopsy of suspected tongue carcinoma 2. Anticipated extubation in the operating room 3. American Society of Anesthesia physical status 1-3 Exclusion Criteria: 1. Rapid Sequence Induction 2. Known or suspected allergy to licorice or its ingredients 3. Liver failure with bleeding disorders 4. Insulin-dependent diabetes mellitus 5. Use of non-steroidal anti-inflammatory drug medication within 24 hours before surgery 6. Chronic opioid use 7. Dementia or inability to use an iv Patient-Controlled-Analgesia (PCA) pump 8. superinfected oropharyngeal tumors 9. Planned postoperative mechanical ventilation or admission to Intensive Care Unit (ICU)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Licorice
ExtractumLiquiritiaeFluidum, 1 g diluted in 30cc water, gargle the solution for 60 seconds without swallowing it starting preoperatively, 3 times a day until post-operative day 3
Sugar water
Sugar gargle: Sirupus Simplex (sugar 5 g) diluted in 30cc water, gargle the solution for 60 seconds without swallowing it starting preoperatively, 3 times a day until post-operative day 3

Locations

Country Name City State
Austria MUVienna Vienna

Sponsors (2)

Lead Sponsor Collaborator
Medical University of Vienna The Cleveland Clinic

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary joint - pain scores and opiate consumption in Post Anesthesia Care Unit (PACU) A joint outcome of average pain score and total opioid consumption between the end of surgery and the first two postoperative hours. Joint hypothesis testing will be used, meaning that Licorice gargling will be deemed better than sugar-water only if found noninferior on both opioid consumption and pain score and superior on at least one of the two. first 2 postoperative hours
Secondary joint - pain scores and opiate consumption on day of surgery Postoperative pain intensity and opioid consumption between the end of surgery and the first postoperative morning. Joint hypothesis testing will be used, meaning that Licorice gargling will be deemed better than sugar-water only if found noninferior on both opioid consumption and pain score and superior on at least one of the two. from end of surgery until the morning of Post-Operative Day (POD) 1
Secondary joint - pain scores and analgesic consumption pain intensity and total analgesics (metamizole or mefenamic acid) consumption in the first three days after surgery. Joint hypothesis testing will be used, meaning that Licorice gargling will be deemed better than sugar-water only if found noninferior on both opioid consumption and pain score and superior on at least one of the two. from surgery conclusion to Post-Operative Day (POD) 3
Secondary postoperative coughing incidence and intensity of postoperative coughing between surgery and the first two hours in the PACU first 2 postoperative hours
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