2%-Mepivacaine With Two Different Vasoconstrictors Solutions in Third Molar Surgery a Comparative Study

Sponsor
University of Sao Paulo (Other)
Overall Status
Unknown status
CT.gov ID
NCT02603198
Collaborator
(none)
30
1
2
23
1.3

Study Details

Study Description

Brief Summary

Dental treatments, particularly third molars extraction, can become extremely uncomfortable and painful. They are associated to anxiety, fear and many other unpleasant sensations. During surgery, patients can present cardiorespiratory repercussions of these sensations. This fact generally justifies the employment of methods of monitoring and appliance of safer therapeutic alternatives. Local anesthetics are the most frequently drugs used in dentistry. Vasoconstrictors, particularly epinephrine, are important components of anesthetic solutions to increased time for anesthetic absorption and consequently increasing the duration of anesthesia. The use of smaller amounts of anesthetic solution can reduce the risk of systemic toxicity, however decrease the total surgical time. It is well known that the amount of epinephrine injected into patients during anesthetic procedures can produce adverse hemodynamic effects. Levonordefrin was adding to dental cartridges promising to reduce cardiac stimulation due it less β activity, and maintain the same clinical and systemic effects. But some studies for maxillary or intraosseous infiltrations showed no difference in heart rate and any anesthetic success over epinephrine. Thus, this study aims to compare the clinical efficacy and safety of anesthetic mepivacaine 2% with epinephrine 1:100,000 or 1:20,000 levonordefrin employing a clinical trial model of third molars extractions in healthy adults.

Condition or Disease Intervention/Treatment Phase
  • Drug: mepivacaine chloridrato epinephrine
  • Drug: mepivacaine chloridrato levonordefrin
N/A

Detailed Description

30 healthy patients, both gender between 18 and 40 years-of-age with the necessity of bilateral third molar removal with similar surgical difficulty will be recruited from a Dental Public University Clinic. Inclusion criteria includes: non-smoking participants, minimum of 50 Kg of weight. After clinical and radiographic examination, they will be randomized accordingly to the side to be operated in two groups: MEPI-LEVO and MEPI-EPI. There will be a memory-washout of 15days between surgeries. In the MEPI-LEVO group, the patient will receive local anesthesia employing 2% chloridrato mepivacaine with 1:20.000 levonordefrin at a maximum of four cartridges of anesthesia. The other side will receive 2%chloridrato mepivacaine with 1:100.000 epinephrine in the same maximum amount. The surgery in both groups will follow strictly patterns of minimum surgical trauma and high cautious antiseptic conditions. The same surgeon will do the tooth extractions but the anesthesia will be done by another oral surgeon in order to blind the type of anesthetic solution from the operator (type of vasoconstrictor used). The amount of bleeding will be quantified just immediately after suture by a blinded observer that will record in a visual analogical scale between 0 and 10 points, where 0 correspond to absence of bleeding and 10 to excessive bleeding.

Blood pressure and heart rate will be accessed in five different moments:
  1. 20minutes before surgical procedure with patients in awaiting room;

  2. 5 minutes before procedure with patient seated in dental chair;

  3. 5 minutes after anesthesia procedure;

  4. during osteotomy/tooth sectioning and

  5. after 10 minutes of suturing.

Patients after surgery will receive a diary to record the time when anesthesia sensation had ended, the amount of analgesics they had consumed and the level of pain in a visual analogic scale. The data will be submitted to statistical analysis with p<0.05 of significance.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
2%-Mepivacaine With Two Different Vasoconstrictors; 1:20.000 Levonordefrin or 1:100.000 Epinephrin for Local Anesthesia in Third Molar Surgery: A Comparative Randomized Clinical Trial
Study Start Date :
Aug 1, 2014
Actual Primary Completion Date :
Jun 1, 2015
Anticipated Study Completion Date :
Jul 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: mepivacaine chloridrato epinephrine

Side of operation that is going to receive anesthesia with 2% mepivacaine chloridrato with 1:100.000 epinephrine, maximum of 4 cartridges

Drug: mepivacaine chloridrato epinephrine
local anesthesia for tooth removal
Other Names:
  • local anesthesia
  • Active Comparator: mepivacaine chloridrato levonordefrin

    Side of operation that is going to receive anesthesia with 2% mepivacaine chloridrato with 1:20.000 levonordefrin, maximum of 4 cartridges

    Drug: mepivacaine chloridrato levonordefrin
    local anesthesia for tooth removal
    Other Names:
  • local anesthesia
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Blood pressure values [20 minutes pre-operatory, 5 minutes before surgery, 5 minutes after anesthesia, 10 minutes after suture]

      assessment of blood pressure values (systolic and diastolic)) in mmHg by a pulse electronic device

    Secondary Outcome Measures

    1. Change in Heart Rate values [20 minutes pre-operatory, 5 minutes before surgery, 5 minutes after anesthesia, 10 minutes after suture]

      assessment of Heart Rate in bpm (beats per minute) by a pulse electronic device

    2. Bleeding [after 1 hour postoperatively]

      Assessment by a visual analogical scale - blinded observer record

    3. Pain [6, 8,24 and 48 hours after suture]

      assessment by visual Analogical Scale - Patient diary

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • minimum body weight of 50Kg, necessity of bilateral impacted third molar removal
    Exclusion Criteria:

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Maria Cristina Zindel Deboni São Paulo Brazil 05508-000

    Sponsors and Collaborators

    • University of Sao Paulo

    Investigators

    • Principal Investigator: Marcelo Minharro Cechetti, PhD, Post - Doctorate

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Maria Cristina Zindel Deboni, Associate Professor, University of Sao Paulo
    ClinicalTrials.gov Identifier:
    NCT02603198
    Other Study ID Numbers:
    • 34147114500000068
    First Posted:
    Nov 11, 2015
    Last Update Posted:
    May 11, 2016
    Last Verified:
    May 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Maria Cristina Zindel Deboni, Associate Professor, University of Sao Paulo
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 11, 2016