Assessment of Oral Health Related Quality of Life After Full Mouth Rehabilitation Under GA

November 8, 2021 updated by: Eyman Sheikh Eldin Mokhtar, Cairo University

Assessment of Oral Health Related Quality of Life After Full Mouth Rehabilitation Under General Anesthesia in a Group of Egyptian Children Below 5 Years Old (A Before and After Study)

To assess Oral health related quality of life (OHRQOL) after full mouth rehabilitation under GA in a group of Egyptian children below 5 years

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Anticipated)

18

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

2 years to 5 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Caregivers paired with their children attending Pediatric Dentistry and Dental Public Health department, faculty of dentistry, Cairo University Egypt

Description

Inclusion Criteria:

  • Age range 2 to 5 years .
  • Children with untreated early childhood caries .
  • Children who will undergo dental treatment under general anesthesia.

Exclusion Criteria:

  • Participation in any other concurrent clinical trials.
  • The presence of serious medical conditions or a transmissible disease such as malignant disease, hepatitis, AIDS etc.
  • Children with special healthcare needs.
  • Children whose parents had no home or mobile phone to enable postoperative contact.
  • Parent that will not sign the consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Oral health related quality of life (OHRQOL)
Time Frame: change from baseline oral health related quality of life at 6 months

Oral health related quality of life (OHRQOL) will be measured by validated questionnaire which is : Early Childhood Oral Health Impact Scale (ECOHIS) .

the unit of measurement is likert scale.

change from baseline oral health related quality of life at 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body mass index
Time Frame: change of baseline body mass at 6 months
Children's weights will be measured in kilograms and heights in meters .Body max index (BMI) will be calculated using this formula: BMI = weight (kg) / height (m)² to report BMI in kg/m^2
change of baseline body mass at 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Fatima Korany, PHD, Cairo university

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

February 1, 2022

Primary Completion (Anticipated)

February 1, 2023

Study Completion (Anticipated)

May 1, 2023

Study Registration Dates

First Submitted

November 9, 2018

First Submitted That Met QC Criteria

November 8, 2021

First Posted (Actual)

November 19, 2021

Study Record Updates

Last Update Posted (Actual)

November 19, 2021

Last Update Submitted That Met QC Criteria

November 8, 2021

Last Verified

October 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • OHRQOL in 5 years children

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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