Bupivacaine in the Treatment of Postoperative Pain of Impacted Third Molar Extraction

Clinical, randomized, experimental, single blind study. The sample for the present study will consist of 40 patients who attend consecutively to maxillofacial surgery, to perform third molar surgical extraction.

The sample size defined for the present study is 40 patients, each with two extractions of third molars for a total of 80 extractions that will be randomized in each patient for the treatment of Bupivacaine and saline respectively.

For the calculation of statistical power with the sample size previously defined to compare the postoperative pain level 4, 12 and 24 hours after the extraction of lower third molars in two groups (Bupivacaine and saline).

With the sample size, investigators defined, calculated, statistical power, test and use, comparison, pain levels, at 4 and 12 hours, with a power greater than 90%. The study will have sufficient power for the study to be conclusive, regardless of whether it finds statistically significant differences or not.

The surgical procedure will be performed by a single oral and maxillofacial surgeon, following the same surgical technique for the extraction of impacted molars, in all patients, including the sulcular flap up to the second molar, with a posterior complementary incision of 45 degrees, without anterior incision Complementary. The osteotomy is performed with a high speed carbide surgical bur. The patients will not receive a previous medication.

In all patients, both impacted lower third molars are surgically removed in one session, beginning the extractions in the right side. Subsequently, one of the alveolus will be irrigated with 4ml of bupivacaine 0.5% with adrenaline vasoconstrictor 1: 200,000 (BUPIROP® 0.5%), the contralateral alveolus will be irrigated with 4 ml of saline solution 0.9% (Baxter laboratories) prior to the placement of the suture for the closure of the surgical wound, using the aspiration to avoid the exit of the medication out of the alveolus.

The decision to use another substance for the irrigation of the alveolus will be taken in a randomized manner.Through numerical assignment according to the order of surgical scheduling. The patients with even numbers are irrigated on the right side with bupivacaine and on the left side with saline. Patients with odd numbers will be irrigated in the opposite way.

Before starting the surgical procedure, the disposable syringes will be marked with their respective content, either bupivacaine 0.5% or saline solution 0.9%, each with 4 ml of the medication.

Patients will be considered blinded to the drug of choice, and patients will not know what type of solution will be administered on each side.

All patients will be medicated with: amoxicillin 500mg every 6 hours for 7 days, acetaminophen 500mg every 6 hours for 5 days, and ibuprofen 400mg every 6 hours for 5 days.

Postoperative pain will be evaluated at 4, 12 and 24 hours after surgery, using the pain visual analog scale from 1 to 10, by telephone call. Patients will be instructed to rate their pain intensity on each side from one to ten.

The information collected in the form will be digitized in a spreadsheet in Excel, to be analyzed in the program IBM® SPSS® version 21. All independent quantitative variables will be summarized by descriptive statistics (average or median, standard deviation o Interquartile range), while qualitative variables will be described with proportions. To compare the pain levels between the two treatments at 4, 12 and 24 hours, the Student's t-test for independent samples or, failing that, the Mann-Whitney U-test will be used.

Prior to this analysis, the normality of the postoperative pain variable (analogous visual scale) will be assessed using the Shapiro Wilk test. A level of significance of 5% will always be assumed for the contrasting statistical tests.

The univariate descriptive analysis will be presented through a summary table. In addition, an error bar graph will be used to show the levels of postoperative pain for each treatment at 4, 12 and 24 hours.

The clinical trial embraces the Declaration of Helsinki of ethical principles for medical research in humans.

Prior to carrying out the study, each of the participants will be explained what the research consists of, participants will be informed about possible adverse reactions to the local anesthetic Bupivacaine, such as drug reaction, altered blood pressure and heart rate, nausea. , vomiting, headaches and allergic skin reactions. At all times there will be a diligent management of the therapy and close observation establish the rules for the handling of personal data in clinical history.

An informed consent will be given to each patient, who will read and explain what is stipulated in it before consenting, to ensure that the participant who signs the informed consent agrees to perform the procedure as stipulated in the statement of the investigation.

The privacy of the individual, subject of investigation, will be protected, identifying it only when the results require it and this authorizes it.

The investigation will be suspended immediately, upon noticing any risk or damage to the health of the subject in whom the investigation is carried out.