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Clinical Trials/NCT03130855
NCT03130855
Unknown
Not Applicable

Buccal Infiltration Technique Compared to Inferior Alveolar Nerve Block Technique for Alleviation of Intraoperative Pain During Pulpal Treatment of Mandibular Primary Molars: A Randomized Controlled Clinical Trial.

Cairo University0 sites48 target enrollmentMay 15, 2017

Overview

Phase
Not Applicable
Intervention
inferior alveolar nerve block with 4% articaine
Conditions
Anesthesia, Local
Sponsor
Cairo University
Enrollment
48
Primary Endpoint
pain experienced by child during pulpal treatment
Last Updated
8 years ago

Overview

Brief Summary

This split mouth randomized control trial is designed as to compare the effectiveness of the buccal infiltration technique with the gold standard inferior alveolar nerve block in anesthetizing mandibular second primary molars to undergoing pulpal treatment.

patient will be videotaped during pulpal treatment of their teeth and an accessing pain will be through an objective pain scale (SEM scale), (sound-eye-motor scale).

the patient will be asked to fill in a subjective Wong Baker pain scale for the pain suffered during injecting the local anesthetic agent in both techniques.

Registry
clinicaltrials.gov
Start Date
May 15, 2017
End Date
August 1, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Omar Sherif Ahmed Abo El Abbas

resident at pediatric dentistry and public health faculty of oral and dental medicine cairo university

Cairo University

Eligibility Criteria

Inclusion Criteria

  • first dental visit.
  • cooperative children (rating 4 or 3 based on Frankl behavior scale) aging from 6 to 8 years suffering from one or more deep carious lesions in their primary molars seeking treatment.
  • Restorable molars with stainless steel crowns.

Exclusion Criteria

  • medically compromised patients. uncooperative children (rating 1 or 2 on the Frankl behavior scale)needing special line of treatment through general anesthesia.
  • signs and symptoms of irreversible pulpitis, spontaneous pain, necrosis or any signs or symptoms of any infection.
  • presence of any radiographic signs of abcess, bone loss, internal or external root resorption.
  • parents or guardians who refuse participating in the study.

Arms & Interventions

inferior alveolar nerve block with 4% articaine

inferior alveolar nerve block using 4% articaine anesthetic solution

Intervention: inferior alveolar nerve block with 4% articaine

buccal infiltration with 4% articaine

buccal infiltration using 4% articaine anesthetic solution

Intervention: buccal infiltration with 4% articaine

Outcomes

Primary Outcomes

pain experienced by child during pulpal treatment

Time Frame: one week

sound-eye-motor

Secondary Outcomes

  • time needed for numbness(one week)
  • pain experienced by the child due to needle prick(one week)

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