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

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Quality of Life

Treatments

Procedure: full mouth rehabilitation

Study type

Observational

Funder types

Other

Identifiers

NCT03497312
OHRQOL in SHCNC

Details and patient eligibility

About

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.

Full 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.

Enrollment

14 estimated patients

Sex

All

Ages

5 to 14 years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

0

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Central trial contact

DUHA M ABDELHAMEED, MASTER; FATIMA KORANY, PHD

Data sourced from clinicaltrials.gov

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