NCT06359093

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,532

participants targeted

Target at P75+ for all trials

Timeline
4mo left

Started Sep 2024

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress84%
Sep 2024Sep 2026

First Submitted

Initial submission to the registry

April 6, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

April 11, 2024

Completed
5 months until next milestone

Study Start

First participant enrolled

September 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2025

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Expected
Last Updated

August 22, 2024

Status Verified

August 1, 2024

Enrollment Period

1 year

First QC Date

April 6, 2024

Last Update Submit

August 20, 2024

Conditions

Keywords

patient-related risk factors

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

Age41 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Faculty of Dentistry

Cairo, Egypt

Location

Central Study Contacts

Rowayda Anwar Eltarawy, MSc

CONTACT

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

Locations