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Completed

NCT Number: NCT04325113

Post Tonsillectomy Analgesia Comparison After Surgery Site Spray of Local Anesthesics

Check analgesia after tonsillectomy in adults

Completed

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Key information

Conditions

Analgesia Agnosia Nervous System Diseases Neurobehavioral Manifestations Neurologic Manifestations Pathological Conditions, Signs and Symptoms Perceptual Disorders Signs and Symptoms

Age range

14 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Javillier

Liège, 4000, Belgium

About this study

We hypothesize that a vaporization of local anesthetics in the tonsil lodge would reduce postoperative pain.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Tonsillectomy

Exclusion criteria

  • Gastric or duodenal ulcer
  • Diabetes
  • Kidney failure
  • Chronic pain and fibromyalgia

Treatment and study plan

Levobupivacaine

Drug

Patient satisfaction and pain score using a visual anagogic scale (VAS)

Other names: xylocaine, Nacl

Primary outcomes

  1. Patient's satisfaction and pain score

    Time frame: until 10 days after the tonsillectomy.

    patient satisfaction and pain score using a visual anagogic scale from 0 (no pain) to 10 (intolerable pain)

Sponsors and collaborators

Lead sponsor

University of Liege

Other

Registry information

Official study title

Post Tonsillectomy Analgesia Comparison After Surgery Site Spray of NaCl 0,9%, Xylocaine 2% or Levobupivacaine 0,5%

Important dates

Study start
2019
Primary completion
2019
Study completion
2020
First posted
Mar 27, 2020
Registry last updated
Mar 27, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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