Efficiency of a Guiding Device for Mandibular Foramen Anesthesia, EZ-Block®, Compared to a Conventional Technique

Sponsor
Elsan (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05214664
Collaborator
(none)
210
5
2
13
42
3.2

Study Details

Study Description

Brief Summary

The success rates reported in the literature for the various truncal anesthesia techniques are extremely variable and have shown a lack of reproducibility of the techniques. The use of the EZ-BLOCK® guidance system would increase this success rate in a significant and reproducible way, as it is based on individualized anatomical foundations and therefore adapted to inter-patient variability.

In order to determine its effectiveness in clinical situations encountered in current practice, a comparative clinical study of the 2 techniques (freehand reference technique and using the EZ-BLOCK® system) is necessary.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Anesthesia
N/A

Detailed Description

The use of loco-regional anesthesia in the mandibular foramen (Inferior Alveolar Nerve Block

  • IANB) is part of the therapeutic arsenal for any Dental Surgeon or specialist in Oral Surgery or Endodontics. These local-regional anesthesias are indicated for restorative, endodontic and single and/or multiple surgical treatments of mandibular teeth homolateral to the infiltrated side. The so-called "conventional" freehand reference technique was described by William Steward Halsted and compared in numerous studies to other truncal anesthesia techniques such as Gow Gates or even Akinosi-Vazirani.

Certain anatomical landmarks must be accurately identified by the operator to reduce the percentage of failure of this technique. Conventional IANB is associated with a 40% failure rate in surgical removal of the lower third molars included, which is the highest percentage of all clinical failures obtained under local anesthesia.

The purpose of this study is to compare the success rate of a IANB guidance device, EZ-Block®, with traditional freehand anatomic administration in the surgical removal of impacted lower third molars.

The use of the EZ-BLOCK® guidance system would increase the success rate significantly and reproducibly because it is based on individualized anatomical foundations and is therefore adapted to inter-patient variability.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
210 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Multicenter, randomized, single-blind, controlled clinical trial with cross-over.Multicenter, randomized, single-blind, controlled clinical trial with cross-over.
Masking:
Single (Investigator)
Masking Description:
In each center, a pair of practitioners has been identified: one practitioner, "Anesthesia", will be in charge of the randomization and the realization of the anesthesia by one of the two techniques described in section 2.2 and 2.3 of the protocol. Another practitioner, "Surgery", will be blinded to the anesthesia technique used. It is this practitioner who will perform the surgical procedure described below.
Primary Purpose:
Other
Official Title:
Efficacy of a Guiding Device for Mandibular Foramen Anesthesia, EZ-Block®, Compared With a Conventional "Freehand" Technique During Mandibular Wisdom Teeth Avulsion.
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Sep 15, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: A guidance system for the realization of a truncal anesthesia close to mandibular foramen

The system consists of a reusable angulator with a tube, a reusable plunger, and a single-use syringe body. These three components are combined with a single-use needle and an anesthetic cartridge to create the ready-to-use EZ-Block® device.

Procedure: Anesthesia
Once the anesthesia is performed by the "Anesthesia" practitioner either with the EZ-Block® device (as described in section 2.2) or by the conventional freehand technique (as described in section 2.3), the surgical procedure will be performed in the same way in both arms, and for each tooth, by the "Surgery" practitioner: The "Surgery" practitioner takes charge of the patient after a post-anesthesia time of 10 minutes and performs a new antisepsis then completes the anesthesia by anesthetizing the buccal and lingual nerve with a carpule of 1.8ml of articaine + adrenaline at 1/200000. The "Surgery" practitioner starts the surgical procedure. In the absence of pain, the practitioner "Surgery" carries out the surgical act in its totality (situation of success for the principal criterion of the study) then records the EVA at the end of the intervention.

Active Comparator: Conventional locoregional anesthesia is performed using osteomuscular landmarks

The injection site is located in the middle of the triangle with an upper base formed, during maximum mouth opening, outside by the mandibular ramus, inside by the mesial pterygoid muscle and above by the lateral pterygoid muscle. The needle is inserted up to the bone contact (about 20mm) while the body of the syringe is directed towards the contralateral premolars or molars. Use of a disposable carpule syringe with aspiration. Use of a 35mm long needle with a 0.5mm diameter. Use of an articaine anesthesia carpule with adrenaline 1/200000.

Procedure: Anesthesia
Once the anesthesia is performed by the "Anesthesia" practitioner either with the EZ-Block® device (as described in section 2.2) or by the conventional freehand technique (as described in section 2.3), the surgical procedure will be performed in the same way in both arms, and for each tooth, by the "Surgery" practitioner: The "Surgery" practitioner takes charge of the patient after a post-anesthesia time of 10 minutes and performs a new antisepsis then completes the anesthesia by anesthetizing the buccal and lingual nerve with a carpule of 1.8ml of articaine + adrenaline at 1/200000. The "Surgery" practitioner starts the surgical procedure. In the absence of pain, the practitioner "Surgery" carries out the surgical act in its totality (situation of success for the principal criterion of the study) then records the EVA at the end of the intervention.

Outcome Measures

Primary Outcome Measures

  1. The success of the truncal infiltration of anesthetic product will be defined as the absence of recourse to additional anesthesia during the procedure [During the procedure]

    The success of the truncal infiltration of anesthetic product will be defined as the absence of recourse to additional anesthesia during the procedure (binary criterion yes / no).

Secondary Outcome Measures

  1. Visual Analog Scale (VAS) of pain [During the procedure]

    Visual Analog Scale (VAS) of pain

  2. Total cumulative dose of anesthetic used [During the procedure]

    Total cumulative dose of anesthetic used

  3. Adverse event report [Up to 10 days after the second intervention]

    adverse event report

Other Outcome Measures

  1. The success of the truncal infiltration of anesthetic product will be compared by center [During the procedure]

    The success rate of the truncal infiltration of anesthetic product will be compared by center

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Male or female, 18 years of age or older

  2. Dental panoramic radiograph or cone beam examination less than 6 months prior to inclusion

  3. Clinical criteria and similar radiographs of the 2 mandibular third molars:

  4. Stage of root planing

  5. Normoposition, horizontal

  6. Type of eruption: disincluded, impacted, impacted

  7. Anatomical relationship between inferior alveolar nerve and mandibular wisdom tooth apices similar for both sides

  8. Affiliation to a social security scheme

  9. Informed consent, dated and signed before any study procedure is performed

Exclusion Criteria:
  1. Pregnant or breastfeeding woman

  2. Known allergy to the anesthetic molecule or to a component of the anesthetic carpule

  3. Contraindication to the use of vasoconstrictor in dental anesthesia

  4. Contraindication to a therapeutic procedure under local anesthesia

  5. Patients taking TKA for another medical reason

  6. Presence of a cystic pathology related to at least 1 of the 2 mandibular third molars to be extracted

  7. Limitation of mouth opening

  8. Associated systemic pathology requiring priority management

  9. Inability of the patient to comply with study follow-up and scheduled visits (especially for second wisdom tooth avulsion)

  10. Patient under legal protection

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Montpellier Montpellier France 34295
2 CHRU Nancy Service d'odontologie Brabois adultes Nancy France 54500
3 Service de médecine bucco-dentaire Hôpital BRetonneau - APHP Paris France 75018
4 Hôpitaux universitaires de Strasbourg Hôpital Civil Pôle de Médecine et chirurgie bucco-dentaires Strasbourg France 67091
5 Odontologie et traitement dentaire Pôle clinique des voies respiratoires Faculté de chirurgie de taire Toulouse France 31059

Sponsors and Collaborators

  • Elsan

Investigators

  • Study Director: Marie-Alix Fauroux, MD, CHU Montpellier - UFR Odontologie de Montpellier

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Elsan
ClinicalTrials.gov Identifier:
NCT05214664
Other Study ID Numbers:
  • EZ-BLOCK
  • 2020-A02755-34
First Posted:
Jan 31, 2022
Last Update Posted:
Mar 28, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 28, 2022