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

Assessment of Oral Health Related Quality of Life After Full Mouth Rehabilitation Under General Anesthesia in a Group of Egyptian Children With Special Health Care Need (A Before and After Study)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03497312
Enrollment
14
Registered
2018-04-13
Start date
2018-12-15
Completion date
2019-06-30
Last updated
2018-06-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality of Life

Keywords

Rehabilitation, children with disabilities, general anesthesia, Children with special healthcare need, handicapped children, full mouth rehabilitation

Brief summary

To assess Oral health related quality of life (OHRQOL) after full mouth rehabilitation under GA in a group of Egyptian children with special healthcare need.

Detailed description

* The study will be conducted in Department of Pediatric Dentistry and Dental Public Health, Faculty of Dentistry, Cairo University, Egypt. * Demographic variables (caregiver age and gender), socio-economic condition, , medical history, and dental history will be collected from the parent or caregiver. The height and weight of each child will be measured in the same manner to standardize the result and their body mass index will be calculated before and after in follow up period. * On the day of the GA, parent or caregiver will complete questionnaires about their child's oral state and well-being over the previous 3 months and oral hygiene instructions will be given to the parent. * The questionnaire will be delivered to the parents/caregivers at baseline and at the 6-month post-operative follow-up visit. Dental examination will be assessed at baseline (pre-operatively) and at 1,3, 6, months post-operative visits.

Interventions

full mouth rehabilitation under general anesthesia

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
5 Years to 14 Years

Inclusion criteria

1. Age range 5 to 14 years. 2. Diagnosed with physical, mental, or sensory disability (separately or combined). 3. Should have a minimum of 12 primary or permanent teeth, or a mixture that had not been treated within the past 12 months.

Exclusion criteria

1. Participation in any other concurrent clinical trials. 2. The presence of serious medical conditions or a transmissible disease such as malignant disease, hepatitis, AIDS etc. 3. Children whose parents had no home or mobile phone to enable post-operative contact. 4. Parent that will not sign the consent.

Design outcomes

Primary

MeasureTime frameDescription
Oral health related quality of life (OHRQOL)at baseline and 6 monthOral health related quality of life (OHRQOL) will be measured by two validated questioner which are : Parental-Caregivers Perceptions Questionnaire (P-CPQ) and family impact scale(FIS). the unit of measurement is likert scale

Secondary

MeasureTime frameDescription
Body massat baseline and 6 monthBody mass will be measure by body mass index,weight and height will be combined to report BMI in kg/m\^2

Contacts

Primary ContactDUHA M ABDELHAMEED, MASTER
duha.hameed.dh@gmail.com00201112096880
Backup ContactFATIMA KORANY, PHD
fatmadent@hotmail.com00201006753265

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026