Diagnostic Accuracy of lncRNA DQ786243 and miRNA146a in Saliva of Oral Potentially Malignant Lesions

NCT ID: NCT05730855

Last Updated: 2023-09-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

45 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-11-01

Study Completion Date

2023-01-23

Brief Summary

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The aim of this study is to evaluate salivary expression of lncRNA DQ786243 as a potential marker for diagnosis of oral potentially malignant lesions compared to normal controls and its effect on salivary expression of miRNA146a.

Detailed Description

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Conditions

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Potentially Malignant Lesions Oral Lichen Planus Leukoplakia, Oral

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Oral Lichen Planus

Real-time Polymerase Chain Reaction technique

Intervention Type DIAGNOSTIC_TEST

Real-time Polymerase Chain Reaction technique

Leukoplakia

Real-time Polymerase Chain Reaction technique

Intervention Type DIAGNOSTIC_TEST

Real-time Polymerase Chain Reaction technique

Healthy control

Real-time Polymerase Chain Reaction technique

Intervention Type DIAGNOSTIC_TEST

Real-time Polymerase Chain Reaction technique

Interventions

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Real-time Polymerase Chain Reaction technique

Real-time Polymerase Chain Reaction technique

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* participants will be divided into 3 groups:

Group I: patients suffering from oral lichen planus Group II: patients suffering from leukoplakia Group III: healthy subjects who are systemically free, non-smokers, and not suffering from any oral mucosal lesions.

Exclusion Criteria

* Subjects taking any drugs inducing any changes that could affect the salivary flow.
* Pregnant females.
* Subjects have any allergies, infectious diseases or active dental abscesses during one month before saliva sampling.
* Patients receiving any drugs related to the oral lesions in the past 6 month prior to sample collection.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Fayoum University

OTHER

Sponsor Role lead

Responsible Party

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Salsabeel

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Fayoum University

Al Fayyum, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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1152014

Identifier Type: -

Identifier Source: org_study_id

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