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Self-Reported Pain in Children Submitted to Single Infiltration of Articaine During Primary Molar Extraction

NCT05443009 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2024-11-25

No results posted yet for this study

Summary

The aim of this study is to analyze the effectiveness of articaine in controlling self-reported pain compared with conventional lidocaine anesthesia in children requiring extraction of deciduous maxillary molars. Only one extraction will be performed on each child. At least two consultations will be necessary to carry out the present controlled, randomized, and blinded study. All participants will be treated by the same dentist. Self-reported pain will be assessed using the Visual Analogue Scale.

Conditions

  • Dental Pain
  • Anesthesia, Local

Interventions

DRUG

Lidocaine

A buccal infiltration injection followed by palatal injections and interpapillary injections of 2% lidocaine with 1:100,000 epinephrine will be administered.

DRUG

Articaine

A single buccal infiltration injection of 4% articaine with 1:100,000 epinephrine will be administered.

Sponsors & Collaborators

  • Universidade Federal de Santa Catarina

    lead OTHER

Principal Investigators

  • Mariane Cardoso, PhD · Universidade Federal de Santa Catarina - UFSC

  • Carla Santana, PhD · Universidade Federal de Santa Catarina - UFSC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
9 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-30
Primary Completion
2024-07-04
Completion
2024-11-21

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05443009 on ClinicalTrials.gov