- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07561606
Correlation Between Posterior Crossbite and Risk of Obstructive Sleep Apnea
Correlation Between Posterior Crossbite and Risk of Obstructive Sleep Apnea: A Questionnaire-Based Analysis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Understanding the correlation between posterior crossbite and OSA risk is essential for early detection and prevention. Pediatric dentists and orthodontists are uniquely positioned to identify craniofacial risk factors and initiate early intervention.
Screening tools such as OSA-18 can help identify children at risk and facilitate timely referral for multidisciplinary management. Furthermore, evaluating this association will contribute to improving clinical decision-making and patient outcomes.
Aim of study:
To assess the correlation between posterior crossbite and the risk of obstructive sleep apnea in children using the OSA-18 questionnaire.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Marwa A. Salmoon, Ph.D
- Phone Number: 01016555055
- Email: maasalmoon@msa.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Children in mixed dentition stage aged 6-12 years
- Presence of posterior crossbite
Exclusion Criteria:
- Syndromic patients
- Previous orthodontic treatment
- Chronic respiratory or neurological disorders Matching criteria and allocation ratio
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
intervention
Screening using the OSA-18 (Obstructive Sleep Apnea-18) questionnaire
|
Screening using the OSA-18 (Obstructive Sleep Apnea-18) questionnaire
|
|
comparator
Patients without posterior crossbite, or Normative OSA-18 scores / low-risk groups
|
Patients without posterior crossbite, or Normative OSA-18 scores / low-risk groups
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Risk or presence of obstructive sleep apnea (OSA) based on OSA-18 scores
Time Frame: 2 months
|
questionnaire
|
2 months
|
Collaborators and Investigators
Investigators
- Study Director: Sally M Mosallam, Master Degree, MSA University
- Principal Investigator: Ahmed Ayman, MSA University
- Principal Investigator: Mohamed Hesham, MSA University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 4-2026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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