search
Back to results

Efficacy of 4% Articaine Terminal Anesthesia in the Lateral Jaw Region in Children

Primary Purpose

Dental Caries, Primary Teeth, Inferior Alveolar Nerve

Status
Completed
Phase
Not Applicable
Locations
Serbia
Study Type
Interventional
Intervention
Tooth extraction of deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years
Endodontic dental treatment of deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years
Conservative tooth restoration of deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years
Sponsored by
University of Novi Sad
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dental Caries focused on measuring Carticaine, Anesthesia, Dental, Pediatric Dentistry

Eligibility Criteria

5 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Respondents of both sexes, aged 5-18 years
  • Subjects in need of either conservative rehabilitation or tooth extraction on deciduous or permanent premolars and / or molars
  • Subjects who have an X-ray of the teeth for the need of dental rehabilitation

Exclusion Criteria:

  • difficult cooperation with the patient
  • existence of allergy to local anesthetic
  • the existence of a diagnosed general disease
  • unsigned informative consent

Sites / Locations

  • Dental Clinic of Vojvodina, Faculty of Medicine, University of Novi Sad

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

The first tasted group using 4% Articaine

The second tasted group using 2% Lidocaine-chloride

Arm Description

The group was divided into three subgroups depending on the age of the participials: 1st group from 5-9 years, 2nd from 10-13 years and 3th from 14-18 years. Following placement of 5% lidocaine topical anaesthetic for 3 minutes prior to and at the site of needle penetration, patients were randomly given one of the following local anesthetic regimes administered by the principle investigator. For indicated dental treatment patients would receive 2.0 ml 4% articaine with 1:100,000 epinephrine as a local infiltration in the mucobuccal region,the lateral region of the lower jaw.Criteria for measuring efficacy would be to measure pain during anesthetic injection, 10 minutes after injection,during and after the intervention. The child's behavior would be monitored through all phases of clinical work by direct observation of the dentist( examiner) using the above methodology. After that, the examiner would fill in the questionnaire based on the answer of the child / parent (guardian).

The group was divided into three subgroups depending on the age of the participials: 1st group from 5-9 years, 2nd from 10-13 years and 3th from 14-18 years. Following placement of 5% lidocaine topical anesthetic for 3 minutes prior to and at the site of needle penetration, patients were randomly given one of the following local anesthetic regimes administered by the principle investigator. For the indicated dental treatment will be used 2.0 ml 2% lidocaine with 1:80,000 epinephrine as an IANB anesthesia for n.alveolaris inferior. Criteria for measuring efficacy would be to measure pain during anesthetic injection, 10 minutes after injection,during and after the intervention. The child's behavior would be monitored through all phases of clinical work by direct observation of the dentist( examiner) using the above methodology. After that, the examiner would fill in the questionnaire based on the answer of the child / parent (guardian).

Outcomes

Primary Outcome Measures

Checkout of painlessness in lateral region lower jaw in children using Visual Analog Scale
Checkout of painlessness in lateral region lower jaw in children using Visual Analog Scale from 0 to 10, where 0 means absence of pain and 10 means unbearable pain.
Checkout of painlessness in lateral region lower jaw in children using tooth vitality test
Control and verification of painlessness of the anesthetized lower jaw region will be performed 10 minutes after anesthetic injection using a tooth vitality test.
Checkout of painlessness in lateral region lower jaw in children using Wong-Baker Pain Rating Scale
Checkout of painlessness in lateral region lower jaw in children using Wong-Baker Pain Rating Scale from 0 to 10, where 0 means absence of pain and 10 means the strongest possible pain.
Checkout of painlessness in lateral region lower jaw in children using Frank Behavior Rating Scale
Checkout of painlessness in lateral region lower jaw in children using Frank Behavior Rating Scale from 0 to 2 , where 0 means cooperating patient and 2 means complete lack of cooperation.
Checkout of painlessness in lateral region lower jaw in children by determining the development of the roots of permanent teeth
By determining the growth and development of the roots of permanent premolars and molars by examiner using x-ray before intervention.
Checkout of painlessness in lateral region lower jaw in children by determining the resorption of the roots of deciduous teeth
By determining the resorption of the roots of deciduous molars by examiner using x-ray before intervention.

Secondary Outcome Measures

Success of indicated dental treatment using tooth vitality test
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using tooth vitality test 10 minutes after dental treatment.
Success of indicated dental treatment using Visual Analog Scale
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using Visual Analog Scale from 0 to 10, where 0 means absence of pain and 10 means unbearable pain.
Success of indicated dental treatment using Wong-Baker Pain Rating Scale
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using Wong-Baker Pain Rating Scale from 0 to 10, where 0 means absence of pain and 10 means the strongest possible pain.
Success of indicated dental treatment using Frank Behavior Rating Scale
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using Frank Behavior Rating Scale from 0 to 2 , where 0 means cooperating patient and 2 means complete lack of cooperation.

Full Information

First Posted
January 11, 2022
Last Updated
January 31, 2023
Sponsor
University of Novi Sad
search

1. Study Identification

Unique Protocol Identification Number
NCT05423392
Brief Title
Efficacy of 4% Articaine Terminal Anesthesia in the Lateral Jaw Region in Children
Official Title
Efficacy of 4% Articaine Terminal Anesthesia in the Lateral Jaw Region in Children: A Double-blind Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
December 2, 2021 (Actual)
Primary Completion Date
January 31, 2023 (Actual)
Study Completion Date
February 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Novi Sad

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Optimal anesthesia is an essential requirement for successful dentoalveolar intervention.To achieve this goal,different anesthetic agents and techniques are available. Inferior alveolar nerve block (IANB) remains the most commonly used anesthetic technique. However, after the worldwide approval of articaine, a relatively new local anesthetic with enhanced tissue diffusion properties, many studies on healthy volunteers have investigated the anesthetic efficacy of buccal articaine infiltration and IANB in the mandibular posterior teeth and reported comparable results. Infiltration anesthesia is technically more straightforward, less stressful to the patient, and associated with higher success and lower complication rates than block anesthesia. The aim of this study was to determine the effectiveness of local infiltration anesthesia using 4% articaine in the analgesia of deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years.
Detailed Description
Clinical study to evaluate the effectiveness of local anesthesia with 4% articaine in order to ensure painless and effective implementation of dental procedures in children. Selection of respondents: participians with good systemic health - patients classified as American Society of Anesthesiologists (ASA) classification - ASA I and ASA II will be included in the study and required invasive dental treatment using local anesthetic (restoration or extraction) on deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years, over 20 kg of body weight.The research would include at least 60 participials aged 5-18, who would be divided into two groups. One group the local anesthetic 4% articaine would be used. The second group would be provided with the local anesthetic 2% lidocaine chloride, as a control group. Analysis and data collection in each group would create subgroups depending on the age of the participials: 5-9 years, 10-13 years and 14-18 years.A clinical study would be doubly blind. Participials who would be included in the clinical study would sign a consent form to participate in the clinical study but would not know which anesthetic would be received.Criteria for measuring efficacy would be to measure pain during anesthetic injection,10 minutes after injection, and during and after the intervention using: Visual Analog Scales (VAS) Tooth vitality test Wong-Baker Pain Rating Scale (W-BFSR) Frank Behavior Rating Scale (FBRS) By determining the growth and development of the roots of permanent premolars and molars By determining the resorption of the roots of deciduous molars. The child's behavior would be monitored through all phases of clinical work by direct observation of the dentist(examiner) who is in charge of measuring the effectiveness of anesthetics but does not know what type of anesthetic. Only a dentist who applies(practitioner) an anesthetic will know what type of anesthetic it is. After that, the examiner would fill in the questionnaire based on the answer of the child / parent (guardian). In accordance with known ethical principles and in accordance with the principles of Good Clinical Practice (GCP), care for the well-being of the patients was maximally respected, in accordance with the latest revision of the Declaration of Helsinki and accepted principles that apply to clinical trials on humans. The holder of the protection of the patients in this clinical trial is the principal researcher, who cooperated with the Ethics Committee of the Dental Clinic of Vojvodina, University of Novi Sad. The patients written Informed Consent implied that the patient had received full information about the research, and was stressed that they had the right to decide independently to participate, without coercion and external influences, or any harmful consequences if they refused to participate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries, Primary Teeth, Inferior Alveolar Nerve, Anesthesia, Dental
Keywords
Carticaine, Anesthesia, Dental, Pediatric Dentistry

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A RANDOMIZED DOUBLE BLIND
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Patients were randomly and equally assigned to treatment groups. The study was planned as a double-blind. Thus, neither the patients nor the researchers knew which anesthetic will be applied. Only practioner, who will injected anesthetic will know what tipe of anesthetic is it - 4% articain or 2% lidocain chlorid. Number of participials is 60, divided into two equal groups.
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
The first tasted group using 4% Articaine
Arm Type
Experimental
Arm Description
The group was divided into three subgroups depending on the age of the participials: 1st group from 5-9 years, 2nd from 10-13 years and 3th from 14-18 years. Following placement of 5% lidocaine topical anaesthetic for 3 minutes prior to and at the site of needle penetration, patients were randomly given one of the following local anesthetic regimes administered by the principle investigator. For indicated dental treatment patients would receive 2.0 ml 4% articaine with 1:100,000 epinephrine as a local infiltration in the mucobuccal region,the lateral region of the lower jaw.Criteria for measuring efficacy would be to measure pain during anesthetic injection, 10 minutes after injection,during and after the intervention. The child's behavior would be monitored through all phases of clinical work by direct observation of the dentist( examiner) using the above methodology. After that, the examiner would fill in the questionnaire based on the answer of the child / parent (guardian).
Arm Title
The second tasted group using 2% Lidocaine-chloride
Arm Type
Active Comparator
Arm Description
The group was divided into three subgroups depending on the age of the participials: 1st group from 5-9 years, 2nd from 10-13 years and 3th from 14-18 years. Following placement of 5% lidocaine topical anesthetic for 3 minutes prior to and at the site of needle penetration, patients were randomly given one of the following local anesthetic regimes administered by the principle investigator. For the indicated dental treatment will be used 2.0 ml 2% lidocaine with 1:80,000 epinephrine as an IANB anesthesia for n.alveolaris inferior. Criteria for measuring efficacy would be to measure pain during anesthetic injection, 10 minutes after injection,during and after the intervention. The child's behavior would be monitored through all phases of clinical work by direct observation of the dentist( examiner) using the above methodology. After that, the examiner would fill in the questionnaire based on the answer of the child / parent (guardian).
Intervention Type
Procedure
Intervention Name(s)
Tooth extraction of deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years
Other Intervention Name(s)
4% Articaine, Effectiveness of anesthetics, Lateral jaw region in children, 2% Lidocaine-chloride
Intervention Description
Tooth extraction will be following up with the methodological procedures in order to define the effectiveness of anesthetics during indicated dental procedure.
Intervention Type
Procedure
Intervention Name(s)
Endodontic dental treatment of deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years
Other Intervention Name(s)
4% Articaine, Effectiveness of anesthetics, Lateral jaw region in children, 2% Lidocaine-chloride
Intervention Description
Endodontic dental treatment will be following up with the methodological procedures in order to define the effectiveness of anesthetics during dental treatment.
Intervention Type
Procedure
Intervention Name(s)
Conservative tooth restoration of deciduous and permanent molars in children aged 5-18 years and mandibular premolars in children aged 10-18 years
Other Intervention Name(s)
4% Articaine, Effectiveness of anesthetics, Lateral jaw region in children, 2% Lidocaine-chloride
Intervention Description
Conservative tooth restoration will be following up with the methodological procedures in order to define the effectiveness of anesthetics during conservative tooth restoration.
Primary Outcome Measure Information:
Title
Checkout of painlessness in lateral region lower jaw in children using Visual Analog Scale
Description
Checkout of painlessness in lateral region lower jaw in children using Visual Analog Scale from 0 to 10, where 0 means absence of pain and 10 means unbearable pain.
Time Frame
during procedure
Title
Checkout of painlessness in lateral region lower jaw in children using tooth vitality test
Description
Control and verification of painlessness of the anesthetized lower jaw region will be performed 10 minutes after anesthetic injection using a tooth vitality test.
Time Frame
10 minutes after anesthetic injection
Title
Checkout of painlessness in lateral region lower jaw in children using Wong-Baker Pain Rating Scale
Description
Checkout of painlessness in lateral region lower jaw in children using Wong-Baker Pain Rating Scale from 0 to 10, where 0 means absence of pain and 10 means the strongest possible pain.
Time Frame
during procedure
Title
Checkout of painlessness in lateral region lower jaw in children using Frank Behavior Rating Scale
Description
Checkout of painlessness in lateral region lower jaw in children using Frank Behavior Rating Scale from 0 to 2 , where 0 means cooperating patient and 2 means complete lack of cooperation.
Time Frame
during procedure
Title
Checkout of painlessness in lateral region lower jaw in children by determining the development of the roots of permanent teeth
Description
By determining the growth and development of the roots of permanent premolars and molars by examiner using x-ray before intervention.
Time Frame
before intervention
Title
Checkout of painlessness in lateral region lower jaw in children by determining the resorption of the roots of deciduous teeth
Description
By determining the resorption of the roots of deciduous molars by examiner using x-ray before intervention.
Time Frame
before intervention
Secondary Outcome Measure Information:
Title
Success of indicated dental treatment using tooth vitality test
Description
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using tooth vitality test 10 minutes after dental treatment.
Time Frame
10 minutes after dental treatment
Title
Success of indicated dental treatment using Visual Analog Scale
Description
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using Visual Analog Scale from 0 to 10, where 0 means absence of pain and 10 means unbearable pain.
Time Frame
immediately after dental treatment
Title
Success of indicated dental treatment using Wong-Baker Pain Rating Scale
Description
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using Wong-Baker Pain Rating Scale from 0 to 10, where 0 means absence of pain and 10 means the strongest possible pain.
Time Frame
immediately after dental treatment
Title
Success of indicated dental treatment using Frank Behavior Rating Scale
Description
The success and effectiveness of anesthetics will be determined immediately after the completion of the indicated dental treatment using Frank Behavior Rating Scale from 0 to 2 , where 0 means cooperating patient and 2 means complete lack of cooperation.
Time Frame
immediately after dental treatment
Other Pre-specified Outcome Measures:
Title
Success of indicated dental treatment using questionnaire
Description
The examiner would fill in a questionnaire ( The guestionnaire for the child / parent (guardian)) wich contains 10 questions with YES or NO answers about the dental procedure and the success of the indicated treatment based on children's responses. Five and more positive answers of ten questions support the positive outcome.
Time Frame
15 minutes after dental treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Respondents of both sexes, aged 5-18 years Subjects in need of either conservative rehabilitation or tooth extraction on deciduous or permanent premolars and / or molars Subjects who have an X-ray of the teeth for the need of dental rehabilitation Exclusion Criteria: difficult cooperation with the patient existence of allergy to local anesthetic the existence of a diagnosed general disease unsigned informative consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Branislav V Bajkin, DMD, PhD
Organizational Affiliation
Dental Clinic of Vojvodina, Faculty of Medicine, University of Novi Sad
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jelena Komšić, DMD
Organizational Affiliation
Dental Clinic of Vojvodina, Faculty of Medicine, University of Novi Sad
Official's Role
Study Director
Facility Information:
Facility Name
Dental Clinic of Vojvodina, Faculty of Medicine, University of Novi Sad
City
Novi Sad
State/Province
Vojvodina
ZIP/Postal Code
21000
Country
Serbia

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29257943
Citation
Majid OW, Ahmed AM. The Anesthetic Efficacy of Articaine and Lidocaine in Equivalent Doses as Buccal and Non-Palatal Infiltration for Maxillary Molar Extraction: A Randomized, Double-Blinded, Placebo-Controlled Clinical Trial. J Oral Maxillofac Surg. 2018 Apr;76(4):737-743. doi: 10.1016/j.joms.2017.11.028. Epub 2017 Nov 27.
Results Reference
result
Citation
Malamed SF, Handbook of Local Anaesthesia, 4th ed. St. Louis: Mosby-Year Book; 1997. pp. 63-64.
Results Reference
result
PubMed Identifier
25885712
Citation
Peedikayil FC, Vijayan A. An update on local anesthesia for pediatric dental patients. Anesth Essays Res. 2013 Jan-Apr;7(1):4-9. doi: 10.4103/0259-1162.113977.
Results Reference
result
PubMed Identifier
29573375
Citation
Alzahrani F, Duggal MS, Munyombwe T, Tahmassebi JF. Anaesthetic efficacy of 4% articaine and 2% lidocaine for extraction and pulpotomy of mandibular primary molars: an equivalence parallel prospective randomized controlled trial. Int J Paediatr Dent. 2018 May;28(3):335-344. doi: 10.1111/ipd.12361. Epub 2018 Mar 24.
Results Reference
result
PubMed Identifier
22924356
Citation
Arrow P. A comparison of articaine 4% and lignocaine 2% in block and infiltration analgesia in children. Aust Dent J. 2012 Sep;57(3):325-33. doi: 10.1111/j.1834-7819.2012.01699.x. Epub 2012 May 28.
Results Reference
result
PubMed Identifier
11733293
Citation
Bijur PE, Silver W, Gallagher EJ. Reliability of the visual analog scale for measurement of acute pain. Acad Emerg Med. 2001 Dec;8(12):1153-7. doi: 10.1111/j.1553-2712.2001.tb01132.x.
Results Reference
result
Citation
Hockenberry MJ, Wilson D, Winkelstein ML. Wongs Essentials of Pediatric Nursing. 7th end. St Louis: Mosby, 2005: 1259.
Results Reference
result
PubMed Identifier
20921070
Citation
Tomlinson D, von Baeyer CL, Stinson JN, Sung L. A systematic review of faces scales for the self-report of pain intensity in children. Pediatrics. 2010 Nov;126(5):e1168-98. doi: 10.1542/peds.2010-1609. Epub 2010 Oct 4.
Results Reference
result
Citation
Champion GD, Goodenough B, von Baeyer CL, Thomas W. Measurement of Pain in Infants and Children, Progress in Pain Research and Management , vol 10. Seattle: IASP Press, 1998: 123-160.
Results Reference
result
PubMed Identifier
21881058
Citation
Meechan JG. The use of the mandibular infiltration anesthetic technique in adults. J Am Dent Assoc. 2011 Sep;142 Suppl 3:19S-24S. doi: 10.14219/jada.archive.2011.0343.
Results Reference
result
PubMed Identifier
8857658
Citation
Oulis CJ, Vadiakas GP, Vasilopoulou A. The effectiveness of mandibular infiltration compared to mandibular block anesthesia in treating primary molars in children. Pediatr Dent. 1996 Jul-Aug;18(4):301-5.
Results Reference
result
PubMed Identifier
18155484
Citation
Jung IY, Kim JH, Kim ES, Lee CY, Lee SJ. An evaluation of buccal infiltrations and inferior alveolar nerve blocks in pulpal anesthesia for mandibular first molars. J Endod. 2008 Jan;34(1):11-3. doi: 10.1016/j.joen.2007.09.006.
Results Reference
result
PubMed Identifier
18436027
Citation
Corbett IP, Kanaa MD, Whitworth JM, Meechan JG. Articaine infiltration for anesthesia of mandibular first molars. J Endod. 2008 May;34(5):514-8. doi: 10.1016/j.joen.2008.02.042.
Results Reference
result
Citation
Srinivasan MR, Poorni S, Nitharshika Y, et al: Articaine buccal infiltration versus lignocaine inferior alveolar block for pulpal anesthesia in mandibular second premolars-Randomized control double blinded clinical trial. J Pierre Fauchard Acad 31:79, 2017
Results Reference
result
PubMed Identifier
20831926
Citation
Meechan JG. Infiltration anesthesia in the mandible. Dent Clin North Am. 2010 Oct;54(4):621-9. doi: 10.1016/j.cden.2010.06.003.
Results Reference
result

Learn more about this trial

Efficacy of 4% Articaine Terminal Anesthesia in the Lateral Jaw Region in Children

We'll reach out to this number within 24 hrs