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The Optimal Injection Site for a 3D Guided Inferior Alveolar Nerve Block Device (IANBD)

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Boston University

Status

Enrolling

Conditions

Inferior Alveolar Nerve Block

Treatments

Procedure: IANBD 3D guided approach

Study type

Interventional

Funder types

Other

Identifiers

NCT06676098
H-43160

Details and patient eligibility

About

Given the thicker cortical bone in the mandible compared to the maxilla, mandibular teeth cannot be effectively anesthetized via local infiltration anesthesia. Instead, clinicians typically perform regional anesthesia and most commonly, Inferior Alveolar Nerve block (IANB). However, the inferior alveolar nerve is deeply submerged by surrounding structures of bone, muscles, ligaments and vessels. Traditional IANB is a technique by using anatomical landmarks not directly related to Inferior Alveolar Nerve (IAN) to approximate the location of mandibular foramen, where IAN enters mandible. IANB is considered a blind technique and known for the lack of accuracy and precision. The failure rate can be as high as 30-45%. In contrast, the investigator's cone beam computed tomography (CBCT) guided IANB device (IANBD) effectively directs the needle to the mandibular foramen which improves the success rate of the IANB on the first attempt, minimizes injection tissue damage, and reduces patient discomfort.

In this proof of concept trial, a 3D printed CBCT guided IANBD will be used to administer anesthesia at three injection sites instead of the traditional IANB technique. Participants will be consented patients at the postdoctoral endodontic treatment center, Department of Endodontics, Boston University (BU) Henry M. Goldman School of Dentistry.

The goal of this research is to to evaluate the acceptability, safety, and effectiveness of guided anesthesia using the IANBD by enrolling 10 subjects who require non-surgical endodontic therapy with a simple, affordable and reliable prototype to be used by clinicians in the dental care setting.

Enrollment

10 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient of Henry M. Goldman School of Dentistry (GSDM)
  • Medical History indicating American Society of Anesthesiology (ASA)1
  • Need Non-surgical Endodontic Therapy on Mandibular Molar or Premolar
  • Asymptomatic pulpal diagnosis (normal, necrotic, asymptomatic irreversible pulpitis, retreatment with no symptoms)
  • The quadrant to be treated must have at least 3 vital teeth.
  • Going to receive a CBCT required for clinical purposes
  • Must be willing to receive guided IANB

Exclusion criteria

  • Allergy to lidocaine or articaine
  • Resin allergy
  • Normal teeth unresponsive to thermal testing (ie calcified chamber)
  • Prior jaw surgery
  • Currently pregnant

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

IANBD guided Inferior Alveolar Nerve block (IANB) injection
Experimental group
Description:
Participants will receive a guided IANB using an IANBD.
Treatment:
Procedure: IANBD 3D guided approach

Trial contacts and locations

1

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Central trial contact

Emily Wen, DDS; Tum-Yi Hsu, DMD DScD

Data sourced from clinicaltrials.gov

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