About this trial
Context: Lidocaine and articaine are two of the most commonly used local anesthetics in dentistry. Lidocaine has often been the anesthetic of choice in clinical practice, but in clinical experience, articaine has proven to be more effective in controlling pain during dental procedures. (Camps-Font, O. et al. 2020).
There are still unanswered questions, such as which of the two local anesthetics is more effective in reducing pain? This could lead us to discuss which one to choose to reduce costs in the dental office.
Objective: The objective of this project is to determine and compare the effectiveness of lidocaine and articaine in clinical contexts such as tooth extraction with infiltrative techniques, seeking to provide answers that will optimize the choice of anesthetic based on the patient and the procedure, thus improving pain management and reducing costs in the dental office.
Design: Randomized double-blind experimental study, parallel groups. The control group received 2% lidocaine, and the experimental group received 4% articaine. The study will be conducted in accordance with the guidelines of the Consolidated Standards of Reporting Trials (CONSORT 2010). The probabilistic sampling technique is through simple randomization. The 100 patients who meet the inclusion criteria will be randomly assigned to the control and experimental groups in a 1:1 ratio.
Expected results: articaine shows a lower percentage of extractions with anesthetic reinforcement and, therefore, a lower average number of additional tubes.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients with clinical indications for simple extraction of upper and lower teeth using infiltrative anesthetic techniques.
Patients without systemic diseases (ASA I)
Patients with controlled systemic disease (ASA II)
Patients with no history of hypersensitivity to anesthetics or their components (epinephrine)
Disqualifiers
Patients with uncontrolled systemic diseases ASA III and pregnant patients.
Patients requiring trunk techniques (Gow gates, Spix, Carrea)
Patients taking medication that affects the anesthetic response (tricyclic antidepressants, anticoagulants)
Patients with a history of neurological or psychiatric disorders that may influence the perception of pain or anxiety.
Trial design
Parallel
Treatments tested in this trial
lidocaine + epinephrine 1:100,000
DrugAdministration of lidocaine as a local anesthetic during dental extraction.
Articaine 4% with epinephrine 1:100,000
DrugAdministration of articaine as a local anesthetic during dental extraction.
Treatment groups
Trial outcomes
Primary outcomes
Number of tubes
continuous quantitative variable
Secondary outcomes
Pain during dislocation using the Visual Analog Scale (VAS) for pain with a minimum of 0 meaning no pain, and a maximum of 10 meaning the most severe pain ever experienced in life.
Continuous quantitative variable
Other outcomes
Age
Continuous quantitative variable.
Sex
Nominal qualitative variable.
Sponsors and contacts
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