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Tooth WearNCT06665191

Prevalence of Tooth Wear and Its Association with Oral Health-related Quality of Life

An observational study of Tooth Wear and Attrition, run by Cairo University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The aim of this study is to detect the prevalence of tooth wear (All forms of cumulative surface loss of mineralized tooth substance loss due to physical and chemico-mechanical process according to the definition of the European Organization for Caries Research (ORCA) and the International Cariology Research Group for… Read more about this study

Who is it for?
Ages 31 to 45 yearsHealthy volunteers can take part
Conditions the study is for
Tooth Wear, Attrition, Erosion
How many people
1,011 participants
Where
No sites listed yet
Study dates
Feb 2026to Nov 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 31 to 45 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Middle aged adult patient attending educational hospital for dental treatments free of charfge

Who may be able to join

  • 1- Patients whose age between 31 to 45 years old. 2- Egyptian 3- Males \& Females 4- Provide informed consent 5- Ability to comprehend asked questions

Who cannot join

  • 1- Patients under or over the selected age group 2- Patients using fixed orthodontic appliances, 3- Patients with special needs

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

omnia Abdellatif omnia Abdellatif Amin, MSC. degree contact

+2 01272512839

omnia.abdellatif@dentistry.cu.edu.eg

About this study

Official title: Prevalence of Tooth Wear, Predictive Risk Factors and Its Association with Oral Health-related Quality of Life Among Middle -aged Adult Patients Attending Dental Educational Hospital At Cairo University: Cross-sectional Study

The aim of this study is to detect the prevalence of tooth wear (All forms of cumulative surface loss of mineralized tooth substance loss due to physical and chemico-mechanical process according to the definition of the European Organization for Caries Research (ORCA) and the International Cariology Research Group for Dental Research (IADR) i.e.: attrition, erosion and abrasion) among middle aged adult patients attending educational hospital at the Faculty of Dentistry, Cairo University and to analyze the distribution of lesions by gender and age, frequency of acidic foods and drinks consumption, medicine usage, chewing habits, systemic diseases, tooth brushing habits, and family socio economic status. Moreover, to evaluate the quality of life among middle aged elderly patients in relation to existence of tooth wear.

The study focuses on middle-aged adult patients (31-45 years) attending the Faculty of Dentistry at Cairo University during 2025-2026. It is an analytical cross-sectional study aimed at assessing the prevalence and risk level of tooth wear using the Basic Erosive Wear Examination Index (BEWE). The BEWE categorizes tooth wear into four levels (0 = no wear, 3 = severe wear), and risk levels are determined by the cumulative score.

Primary outcome: the prevalence of tooth wear and associated risk levels. Secondary outcomes: identifying predictive risk factors and assessing the Oral Health Impact Profile (OHIP) for patients diagnosed with tooth wear. All participants will be examined, and those with a BEWE score above 0 will be considered affected. Risk levels will be stratified as no risk, low, medium, or high.

Being tested
No Intervention: Observational study for prevalence of dental wear and its association with quality of life
Keywords
Tooth wear, attrition, BEWE, Basic erosive wear examination, quality of life
Medical subject headings
Tooth Wear

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No Intervention: Observational study for prevalence of dental wear and its association with quality of lifeOther

    not applicable as it is an observational study testing the prevalence of dental wear in patients attending Cairo University

Study groups in NCT06665191
Study groupRoleWhat they receive
Middle aged Adults NOT suffering from dental wearMiddle aged Adults NOT suffering from dental wear attending dental educational hospital in Cairo University
Middle aged adults Suffering from dental wearMiddle aged adults Suffering from dental wear attending dental educational hospital in Cairo University
Receives: Other: No Intervention: Observational study for prevalence of dental wear and its association with quality of life

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prevalence and risk level of tooth wear

    Prevalence of wear will be tested using Basic erosive wear examination index (BEWE) 0 =no tooth wear

    1. =minimal loss of surface texture
    2. = distinct defect, hard tissue loss <50% of the surface area
    3. = hard tissue loss ≥ 50% of the surface area The examination is repeated for all teeth in a sextant but only the surface with the highest score is recorded for each sextant.

    To calculate prevalence Examined participants with score 0 will represent unaffected population % Examined participants with scores above 0 will represent the affected population % Stratification of risk levels will be done for affected population according to BEWE risk levels. The sum of the scores is calculated to provide the BEWE risk level (0-14) 0-2 = no risk 3-8= low risk 9-13= medium risk 14= high risk

    Measured: 1 year

Secondary outcomes (2)
  1. • Predictive risk factors for all participants using a questionnaire

    Sociodemographic data:

    age, gender, occupation and education

    Predictive risk factors:

    1. Frequency of consuming acidic food and fruits, carbonated beverages and alcohol.
    2. Medicine usage ( vitamin c, aspirin)
    3. Chewing habits
    4. Systemic diseases
    5. Tooth brushing habits
    6. Family socio economic status.

    Measured: 1year

  2. Oral Health-Related Quality of Life (OHRQoL) using a questionnaire

    OHRQoL will be measured using Oral Health Index Profile (OHIP-14) questionnaire

    OHIP-14 is a 14-item questionnaire that measures :

    Functional limitation Physical pain Phycological discomfort Physical disability Social disability Phycological disability Handicap

    It measures responses on a Likert scale (0-4) with the following values:

    Never (0) Hardly ever (1) Occasionally (2) Frequently (3) Very frequently (4) Points for each response are summed so that each patient can score a minimum of 0 points and a maximum of 56 points. Low scores indicate better self-perceived quality of life, and high scores indicate worse self-perception of oral quality of life Participants diagnosed with tooth wear

    Measured: 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Oct 2024
  2. Study startFeb 2026 (estimated)
  3. Primary completionOct 2026 (estimated)
  4. Study completionNov 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrolment
1,011 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06665191
Sponsor's protocol ID
1441991
Status last verified
Oct 2024
First submitted
9 Oct 2024
Last updated
30 Oct 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Tooth Wear and Attrition, run by Cairo University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 30 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact omnia Abdellatif omnia Abdellatif Amin, MSC. degree (+2 01272512839, omnia.abdellatif@dentistry.cu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prevalence and risk level of tooth wear (time frame: 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Oct 2024.

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