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NCT05678153 Clinical Trial

Effect of Passive Smoking on Orofacial Dysfunction Among a Group of Egyptian Children: A Cohort Study

Smoking Clinical Trial

— ACU222  

Official title:
Effect of Passive Smoking on Orofacial Dysfunction Among a Group of Egyptian Children: A Cohort Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05678153
Other study ID # ACU 222
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 1, 2023
Est. completion date June 15, 2023

Study information
Verified date March 2023
Source Ahram Canadian University
Contact Mennat Allah Abd-Elsabour, Master
Phone 00201026022605
Email menna.alkaram@acu.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to investigate the orofacial dysfunction in children who are subjected to passive smoking and to correlate its results to their saliva cotinine levels

Description:

The participants will be recruited from the pedodontics outpatient clinic in the, Faculty of Oral and Dental Medicine, Ahram Canadian University, Egypt. The aim and the steps of the study will be explained to the guardian. After obtaining the informed consent, the investigator will fill an administrative questionnaire, which includes parents and child's personal data, medical and dental history, a question inquiring if one of the parents smokes in the house, the frequency of smoking, smoking type, and number of cigarettes (if present). Then, the examination of orofacial dysfunction will be evaluated by the investigator, using Nordic Orofacial Test - screen (NOT-S)

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 20
Est. completion date June 15, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 7 Years
Eligibility Inclusion Criteria: - Children who are free from any systematic disease, or genetic disorders that - Children whose families accept to participate in this study. Exclusion Criteria: - Children whose parents quit smoking after the child was born.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Nordic Orofacial Test-Screen (NOT-S)
screening tool to detect orofacial dysfunction

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Ahram Canadian University

Outcome
Type Measure Description Time frame Safety issue
Primary Orofacial Dysfunction (measured using Nordic Orofacial Test-Screen) deviation from normal functions of facial and oral structures baseline record
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