Buccal Infiltration Technique Compared to Inferior Alveolar Technique

Buccal Infiltration Technique in Comparison to the Inferior Alveolar Nerve Block Technique for Anesthetizing Mandibular Primary Molars During Pulpal Treatment

This study was conducted to compare the efficacy of the buccal infiltration technique with inferior alveolar nerve block technique for alleviation of intraoperative pain during pulpal treatment of second mandibular primary molars using 4% Articaine 1:100000.

The study started with 22 cooperative medically free patients aging 7 to 8 years old seeking treatment for bilateral deep carious mandibular second primary molars with no previous history of irreversible pulpitis, swelling, sinus tract or tooth mobility.

Randomization was achieved when each candidate was instructed to pick an opaque and sealed envelope from two separate black and opaque boxes. First box contained two envelopes to identify the side on which the operator will perform the treatment. While the second box contained another two envelopes describing which anesthetic technique will be implemented with the previously chosen side.

After clinical and radiographic examination, the patient received the pulpal treatment under the identified side and injecting technique. Videotaping of the pulpal treatment procedure was initiated after numbness was experienced by the child.

A blind assessor was assigned to review the videos and fill in the SEM pain scale to identify the pain and level of discomfort experienced by the child during the pulpal treatment.

Study Overview

• Status: Recruiting
• Conditions: Local Anesthetic Complication
• Intervention / Treatment: Other: Inferior alveolar nerve block technique; Other: Buccal infiltration technique

Detailed Description

This study was a split mouth randomized controlled trial enrolling 22 patients from the diagnostic center in the Pediatric Dentistry and Dental Public Health Department Faculty of Dentistry, Cairo University. All participants met the following inclusion criteria:

1. Cooperative children (rating four or three based on Frankl behavior scale) aging from seven to eight years.
2. Medically free child categorized as ASA I or ASA II according to the American Society of anesthesiologist.
3. Restorable bilateral deep carious lower primary second molars as shown in figure (1).
4. Normal radiographic findings.

Preoperative periapical x-rays were done on the targeted molars to confirm their adherence to the eligibility criteria and to confirm their restorability.

Each participant was asked to pick an opaque and sealed envelope from two separate black and opaque boxes to randomly choose the operated technique and side on the first operating visit. By default the other technique will be implemented on the other side on the upcoming visit.

Proper psychological management and desensitization procedures were undertaken to prepare the patient for the treatment. Certain phrases were used to prepare the child for applying topical anesthetic gel and injecting the anesthetic agent in any given technique like "The magic water will be used to put the tooth to sleep".

The protocols followed for inferior alveolar nerve block and buccal infiltration techniques were according to Jones and Dean; 2016 and Tudeshchoie et al; 2013.

Caries removal and pulpal treatment were videotaped with both local anesthetic techniques. Caries was removed using a high speed contra with copious cooling and proper suction, complete deroofing and excavation to the coronal pulpal tissues, bleeding from canals was evaluated after the application of a wet cotton for two to four minutes, and then a cotton damped with formocresol was applied for two to four minutes, fixation and brown stumps had to be evident for applying the zinc oxide and eugenol dressing in the pulp chamber.

If any pain was felt during the procedure and the patient raised his/her left hand the procedure was immediately halted. If pulpal exposure was still not evident additional anesthesia was injected through the inferior alveolar nerve block technique since it is the gold standard for anesthetizing mandibular posterior teeth. While if pain was experienced after pulpal exposure few drops of anesthesia was injected intra-pulpally, in both cases and this was considered a failure in the anesthetic technique used.

After application of zinc oxide and eugenol cement, video recording was halted, zinc phosphate cement was then used to seal the coronal part of the tooth and then the tooth was covered with a preformed stainless steel crown.

Videos were then assessed by an assessor who was completely blinded from the technique of injection to fill in a printed (SEM) pain scale sheet for each technique with each participant.

Postoperative instructions were verbally stated to the parent/guardian regarding precautions towards lip biting due to lip numbness. The patient was dismissed, and after at least a week the patient would be recalled to operate on the contralateral side.

In order to ensure complete blindness of the statistician to the results of the local anesthetic techniques, the inferior alveolar nerve block technique (IANB) was designated as Treatment Group I and buccal infiltration technique (BI) was designated as Treatment Group II.

B. Data measurement:

SEM Pain Scale was used to evaluate the intraoperative pain experienced during pulpal treatment of mandibular primary second molars with both local anesthetic techniques using articaine four percent solution.

• Study Type: Interventional
• Enrollment (Anticipated): 22
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: abbas O Sherif, Master Degree holder; Phone Number: Manial 01210965669; Email: omar_aboelabbas0107@yahoo.com

Study Locations

• Egypt
  • Manial
    • Cairo, Manial, Egypt
      • Recruiting
      • Cairo University
      • Contact: hany M Saber, Associate Professor; Phone Number: 01225519667; Email: drhanysaber@yahoo.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 7 years to 8 years (Child)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Cooperative children (rating 4 or 3 based on Frankl behavior scale) aging from 7 to 8.
2. Medically free child ASA I or ASA II according to the American Society of anesthesiologist.
3. Restorable bilateral deep carious lower primary second molars.
4. Normal radiographic findings.

Exclusion Criteria:

• 1- Uncooperative child (rating 1 or 2 on the Frankl behavior scale). 2- Signs and symptoms of irreversible pulpitis, spontaneous pain, necrosis or any signs and symptoms of abscess.

  3- Radiographic signs of abscess, bone loss, internal or external root resorption was evident.

  4- Parents or guardians refused participating in the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: buccal infiltartion technique; local anesthetic technique	Other: Inferior alveolar nerve block technique; a technique for injecting local anesthetic solution to anesthetize the inferior alveolar nerve
Active Comparator: Inferior alveolar nerve block technique; local anesthetic technique	Other: Buccal infiltration technique; a technique for injecting local anesthetic solution in the buccal mucobuccal fold between the roots of the targeted tooth

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pain during pulpal treatment	Sound Eye Motor SEM Pain scale	up to one month

Collaborators and Investigators

• Sponsor: Cairo University
• Investigators: Study Director: Saber H Mohamed, Associate Professor, Cairo U

Study record dates

Study Major Dates

• Study Start (Actual): March 1, 2021
• Primary Completion (Anticipated): October 1, 2022
• Study Completion (Anticipated): December 1, 2022

Study Registration Dates

• First Submitted: March 14, 2021
• First Submitted That Met QC Criteria: March 20, 2021
• First Posted (Actual): March 23, 2021

Study Record Updates

• Last Update Posted (Actual): August 2, 2022
• Last Update Submitted That Met QC Criteria: July 30, 2022
• Last Verified: July 1, 2022

More Information

Terms related to this study

• Other Study ID Numbers: BI vs IANB

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No