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Not yet recruitingNCT06359093Updated Aug 22, 2024

Prevalence Of Non-Carious Cervical Lesions, Associated Risk Indicators and Salivary Assessment Among Middle Adulthood Patients.

An observational study in Non-carious Cervical Lesions, sponsored by Cairo University. Not yet recruiting at 1 site in Egypt. Open to participants aged 41 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-22.

Sponsored by Cairo University · Observational

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year 1 month ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
1,532
Ages
41 Years to 60 Years
Sex
All
01

Study 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.

Read the detailed description

Dental patients will be recruited from diagnostic central clinic at the Cairo University Dental Educational Hospital. Oral examination will be done, the full aim of the study will be explained to the patient, and patient acceptance is a must. The questionnaire will be filled by patients including age, gender, occupation, education, place of residence, toothbrushing: included frequency, method, intensity, hardness and duration, biting and chewing habits, medical history [related to gastrointestinal problems such as belching, heartburn, vomiting, gastro-oesophageal reflux (GER), peptic ulcer disease], eating disorders (anorexia, bulimia), medication list, frequency of consuming acidic food and fruits, carbonated beverages and alcohol and smoking status. Salivary assessment regarding flow rate and pH for a subgroup diagnosed with non-carious cervical lesions.

02

Conditions studied

  • Non-carious Cervical Lesions

Keywords

  • patient-related risk factors
03

In context

Uterine Cervical Diseases

53 studies on the registry are indexed under Uterine Cervical Diseases; 11 are open to participants now.

This study's planned enrollment of 1,532 is above the median of 1,215 across 10 observational studies indexed under Uterine Cervical Diseases.

Browse Uterine Cervical Diseases studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
41 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Middle adulthood patients (41-60 years old) attending Diagnostic central clinic at the Cairo University Dental Educational Hospital.

Inclusion criteria

  1. Patients whose age between 41-60 years old.
  2. Patient consulting in the outpatient clinic
  3. Provide informed consent.
  4. Males \& Females
  5. Egyptian

Exclusion criteria

Exclusion Criteria:

  1. Patients under or over this age group.
  2. Refuse to participate in the study.
  3. Wearing orthodontic appliance.
  4. The presence of trismus.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
1,532 participants (estimated)
Patient registry
No
06

What researchers measure

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

    Time frame: 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.

    questionnaire will be used to collect data. For quantitative analysis of saliva: if saliva flow rate is less than 1ml/min , it is considered xerostomia. If saliva flow rate is less than 1ml/min , it is low salivary flow if saliva flow rate is more than 3, it is high salivary flow

    Time frame: Day 1

07

Study locations

1 site
  • Faculty of Dentistry
    Cairo, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06359093
Lead sponsor
Cairo University
Responsible party
Rowayda Anwar Hosny Eltarawy (Assistant Lecturer, Cairo University) — Principal investigator
First posted
Apr 11, 2024
Start date
Sep 2024 (estimated)
Primary completion
Sep 2025 (estimated)
Completion
Sep 2026 (estimated)
Last update
Aug 22, 2024

Study contacts

Rowayda Anwar Eltarawy, MSc
Contact
rowayda.anwar@dentistry.cu.edu.eg
+201066517727

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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