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Efficiency of Sonic Activation During Root Canal Treatment of Primary Molars on Postoperative Pain and Facial Expressions

NCT07138937 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-09-12

No results posted yet for this study

Summary

This study was conducted to evaluate the efficiency of sonic activation of 5%sodium hypochlorite during root canal treatment of primary molars on postoperative pain and facial expressions. In addition to comparing between the Five-face pain scale and AI Emotion Detector mobile application in postoperative pain assessment.

Conditions

  • Root Canal Treatment in Children Primary Molars
  • Postoperative Pain
  • Facial Expressions
  • Facial Emotions
  • Artificial Intelligence Mobile Application
  • Sonic Activation

Interventions

PROCEDURE

Root canal treatment in primary molars with irreversible pulpitis

Root canal treatment in primary molars with irreversible pulpitis followed by coronal restoration with stainless-steel crowns in a single visit.

DEVICE

EDDY system for sonic activation of irrigation

sonic activation of irrigation with EDDY system during root canal treatment in primary molars

DEVICE

side-vented needle

conventional irrigation with side-vented needle without activation during root canal treatment in primary molars

Sponsors & Collaborators

  • Suez Canal University

    lead OTHER

Principal Investigators

  • Ghada Abdelhamid El-Baz, Professor of Pedodontics · Faculty of dentisrty, Suez Canal University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
5 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-08-01
Primary Completion
2025-01-01
Completion
2025-03-01

Countries

  • Egypt

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 NCT07138937 on ClinicalTrials.gov