Does Treating Early Childhood Caries Under Local or General Anesthesia Have Varying Effects on OHRQoL

NCT ID: NCT05761691

Last Updated: 2023-03-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

73 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-02-01

Study Completion Date

2022-03-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

A two-arm randomized control trial is to compare the changes in OHRQoL scores among children treated for ECC under general (DGA) and local anesthesia (LA). Outcome variable was OHRQoL, measured using the early childhood oral health impact scale ECOHIS and explanatory variable was the administration of local or general anesthesia.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Ethical Approval:

The study proposal was registered with the research center at Riyadh Elm University (REU), Riyadh, Saudi Arabia, and ethical approval was obtained from the institutional review board (IRB). Informed consent was obtained from the parents of all participants and the data was managed such that complete confidentiality of the patient was maintained. The current study abides by the regulations presented at the Helsinki declaration.

Sample size calculation:

The sample size required to reject the null hypothesis was estimated using the data from a previous study42 wherein 33.3% of the children with treatment under DGA were reported with better OHRQoL in contrast to 3.3% in the control group. With the alpha set at 0.05, the 80% power of study, and the addition of 30% dropout rate, a sample size of a minimum of 50 children in each group was estimated.

Sample selection criteria:

Arab children aged six years or younger, who were recommended for comprehensive dental treatment at Riyadh Elm university hospitals (Munseah and Numthjiah campuses) by pediatric dentistry residents, and who consented to be part of the study were recruited. Before subjecting the recruited participants to randomization, the intraoral findings were documented, radiographs were taken, and a plan of treatment was designed. Children with systemic disease, physical and mental disability, and congenital defect such as amelogenesis imperfecta or cleft lift/palate were excluded.

Study variables:

The OHRQoL was measured using the Arabic version of the Early childhood impact scale ECOHIS.35 This scale has 13 questions and is divided into the child and family impacts. The child impact part includes nine questions under four fields: child OH symptoms, function, psychology and self-image, and social interaction while the family impact part contains four questions under two domains: parental distress and family function.35 Parents responded to the questions on a 6-point Likert scale (0, never; 1, hardly ever; 2, occasionally; 3, often; 4, very often; and 5, do not know). The overall score was calculated by summing the scores of each item and domain separately. Lower scores indicated better OHRQoL

Explanatory variables:

The primary explanatory variable was the administration of local or general anesthesia to perform the comprehensive dental treatment which included pulp therapy, restoration, and extraction of primary teeth. Age and gender of children, family socio-economic status, parent's education level, dental index "dft" decayed and filled teeth, along with fractured and traumatized teeth were also recorded. The details related to clinical examination, dental history, and treatment provided were recorded from the electronic file system "DENTPLUS" at REU hospitals. The average number of dental visits was required to finish the treatment plan in LA group around five to six while in GA group the treatment was provided as a day care surgery for healthy child patients.

Data collection process:

The data collection was carried out from April 2021 to January 2022. During the Child's first appointment, an oral examination was conducted, followed by a comprehensive treatment plan. Additionally, the child's behavior was assessed using the Frankel behavior rating scale before subjecting them to randomization.Each eligible child with no behavioral issues was subjected to a flip coin randomization process and assigned accordingly into the LA or DGA group. The process of flip coin method to assign the children into two groups was carried out until one group reached the required sample size of 50, and then the remaining eligible children were assigned to the subsequent group. Importantly, therapy under LA was planned for children whose parents were fearful and did not consent for DGA. Also, therapy under DGA was planned for children whose parents wanted to complete the treatment in a single session. These children who could not be subjected to randomization process were treated but not included in the study.

In this study, due to obvious reasons, the child-parent duo and the primary investigator performing the dental treatment could not be blinded to the intervention. However, to somewhat follow the blinding process, the primary investigator asked a trained dental auxiliary staff, who was not part of the study, to administer the ECOHIS questionnaire and collect the socio-demographic data. This process where the primary investigator was blinded to the assessment of the outcome variable was followed at the baseline, one week, and one-month data collection timelines. The person carrying out the statistical analyses was blinded to the intervention and the outcome assessment. All the data was first entered in the Microsoft Excel and then transferred to SPSS version 24 (IBM, USA) for data analyses.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Oral Health Related Quality of Life OHRQoL

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two armed RCT was planned.

First: children received dental treatment under general anesthesia (Study group)

Second: Children received dental treatment under local anesthesia (Control group) in regular dental sitting.
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Children treated for Early childhood caries under general anesthesia (DGA)

GA group (Study group) the dental treatment was provided as a day care surgery under general anasthesia for healthy child patients.

Group Type EXPERIMENTAL

Dental treatment

Intervention Type PROCEDURE

Children treated for ECC under general (DGA) and local anesthesia (LA).

Children treated for Early childhood caries under Local anesthesia (LA)

LA goup (control group) the average number of dental visits was required to finish the treatment plan in local anasthesia group around five to six visits.

Group Type EXPERIMENTAL

Dental treatment

Intervention Type PROCEDURE

Children treated for ECC under general (DGA) and local anesthesia (LA).

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Dental treatment

Children treated for ECC under general (DGA) and local anesthesia (LA).

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Arab children
* Age six years or younger

Exclusion Criteria

* Children systemic disease
* Children with physical and mental disability
* Children with congenital dental defect such as amelogenesis imperfecta
* Children with cleft lift/palate
Minimum Eligible Age

2 Years

Maximum Eligible Age

6 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Riyadh Elm University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mohammad Abdullah Alwadaani

Pediatric Dental Resident

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Mohammad Alwadaani, MSc

Role: PRINCIPAL_INVESTIGATOR

Riyadh Elm University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Riyadh Elm University

Riyadh, , Saudi Arabia

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Saudi Arabia

References

Explore related publications, articles, or registry entries linked to this study.

Alwadani MA, Alsulaiman DA, Kakti A, Alamoudi S, Tadakamadla SK, Quadri MFA. Comparison of Oral Health-Related Quality of Life scores in children treated for early childhood caries under general and local anesthesia: a quasi-experimental study. Eur Arch Paediatr Dent. 2023 Dec;24(6):719-728. doi: 10.1007/s40368-023-00835-w. Epub 2023 Aug 29.

Reference Type DERIVED
PMID: 37644356 (View on PubMed)

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

FBGRP-2021-562-421-415

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Treating Children With Extensive Dental Needs
NCT06863103 ENROLLING_BY_INVITATION
Use of Fissure Sealants on Primary Molars
NCT01438866 COMPLETED PHASE4
Effect of Dental Treatment on Children's Growth
NCT01243866 COMPLETED PHASE1/PHASE2