Actively Recruiting

Phase Not Applicable
Age: 4Years - 6Years
All Genders
NCT06623851

Digital Versus Conventional Impression on Discomfort and Dental Anxiety Among Preschoolers

Led by Hams Hamed Abdelrahman · Updated on 2024-10-02

66

Participants Needed

1

Research Sites

14 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Background: Taking alginate impressions for preschoolers is challenging and might be disturbing for them. Therefore, intraoral scanners are suggested as a better alternative to the conventional alginate impression. Objectives: The present study aims to evaluate and compare the level of patients' discomfort, dental anxiety, gag reflex, behavior and time required for taking alginate impressions with that of intraoral scanning. Materials and methods: The study will be a randomized, controlled clinical trial, parallel design. A total of 666 pediatric dental patients aged from 4-6 years will be selected from the outpatient clinic of the of Pediatric Dentistry and Dental Public Health Department, Faculty of Dentistry, Alexandria University. Participants will be allocated into 2 groups. Children in the first group will receive digital impressions by an intraoral scanner, while those of the second group will receive conventional alginate impressions. Patients' discomfort will be evaluated by a modified VAS index supported with emojis. Dental anxiety will be evaluated using Facial Image Scale (FIS). Gag reflex will be assessed by Gag Severity Index (GSI). Child's behavior towards the impression technique in the 2 groups will be evaluated using Venham's Behavior rating scale. Time taken to complete the procedures will be recorded using a digital stopwatch.

CONDITIONS

Official Title

Digital Versus Conventional Impression on Discomfort and Dental Anxiety Among Preschoolers

Who Can Participate

Age: 4Years - 6Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 4 to 6 years
  • Children with scores of 3 or 4 on the Frankl Behavioral Rating Scale before treatment
  • Children with no previous dental experience
  • Parents have signed informed consent for participation
Not Eligible

You will not qualify if you...

  • Any physical or mental disability or psychological problems
  • Children with temporomandibular joint or periodontal discomfort

AI-Screening

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Trial Site Locations

Total: 1 location

1

Alexandria Faculty of Dentistry

Alexandria, Egypt

Actively Recruiting

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Research Team

A

Arwa Ghoneim, BDS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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