- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07390188
Prevalence of Oral Mucosal Lesions Among a Sample of Adult Egyptian Subjects
January 29, 2026 updated by: Eslam EL Sayed Abdelfattah El Zayat, Cairo University
Prevalence of Oral Mucosal Lesions Among a Sample of Adult Egyptian Subjects: Hospital Based Cross-sectional Study.
Oral mucosal lesion represents a wide array of conditions.
They may be the result of a local or systemic infection or trauma or the manifestations of a medical condition or neoplastic growth weather primary or metastatic or may be mistaken for a variation of a normal structure.
This study aims to estimate the prevalence of OMLs and describe the risk factors for the development of OMLs in a sample of the Egyptian population Research Question :What is the prevalence of oral mucosal lesions and their associated risk factors in a sample of adult Egyptians?
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
14645
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Eslam El Zayat, BSC of Oral & Dental Medicine
- Phone Number: +201062630864
- Email: eslam.elzayat@dentistry.cu.edu.eg
Study Locations
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-
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Cairo, Egypt
- Recruiting
- Cairo University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Individuals, above 18 years old, presenting for initial diagnosis to DC of outpatient clinic of Faculty of Dentistry, Cairo university.
Description
Inclusion Criteria:
- Adults, 18 years old and above, Egyptian individuals
Exclusion Criteria:
- Individuals refusing to participate in the study. Individuals unable to give accurate or full information due to suffering from acute symptoms, requiring immediate intervention. Individuals unable to give accurate or full information due to any disease preventing them from opening their mouth.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Lesion Presence
Time Frame: At Time of enrollment
|
At Time of enrollment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 8, 2025
Primary Completion (Estimated)
April 30, 2026
Study Completion (Estimated)
May 30, 2026
Study Registration Dates
First Submitted
January 29, 2026
First Submitted That Met QC Criteria
January 29, 2026
First Posted (Actual)
February 5, 2026
Study Record Updates
Last Update Posted (Actual)
February 5, 2026
Last Update Submitted That Met QC Criteria
January 29, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- OMED 1.1.1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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