Prevalence Of Non-Carious Cervical Lesions, Associated Risk Indicators and Salivary Assessment Among Middle Adulthood Patients.
1 other identifier
observational
1,532
1 country
1
Brief Summary
The aim of this study is to describe the prevalence of non-carious cervical lesions in middle adulthood patients attending the Cairo University Dental Educational Hospital and to analyze the distribution of lesions by gender and age, tooth functional group, jaw, arch side and tooth surface. Moreover, to explore the associated risk indicators of the lesions as well as the flow rate and pH of saliva, as one of the potential etiological factors, will be assessed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2024
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 6, 2024
CompletedFirst Posted
Study publicly available on registry
April 11, 2024
CompletedStudy Start
First participant enrolled
September 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
ExpectedAugust 22, 2024
August 1, 2024
1 year
April 6, 2024
August 20, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Prevalence of non-carious cervical lesions (NCCLs) in Middle adulthood patients (41-60 years old) attending Diagnostic central clinic at the Cairo University Dental Educational Hospital.
clinical examination
Day 1
Secondary Outcomes (1)
Associated risk indicators for all participants. 3.Salivary assessment regarding flow rate and pH for subgroup diagnosed with non-carious cervical lesions.
Day 1
Eligibility Criteria
Middle adulthood patients (41-60 years old) attending Diagnostic central clinic at the Cairo University Dental Educational Hospital.
You may qualify if:
- Patients whose age between 41-60 years old.
- Patient consulting in the outpatient clinic
- Provide informed consent.
- Males \& Females
- Egyptian
You may not qualify if:
- Patients under or over this age group.
- Refuse to participate in the study.
- Wearing orthodontic appliance.
- The presence of trismus.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Faculty of Dentistry
Cairo, Egypt
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Lecturer
Study Record Dates
First Submitted
April 6, 2024
First Posted
April 11, 2024
Study Start
September 1, 2024
Primary Completion
September 1, 2025
Study Completion (Estimated)
September 1, 2026
Last Updated
August 22, 2024
Record last verified: 2024-08