Validation of Salivary Proteomic Biomarkers for Early Detection of Oral Cancer in Egyptian Population

NCT ID: NCT06471270

Last Updated: 2024-06-24

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

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-07-15

Study Completion Date

2024-03-15

Brief Summary

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The present investigation was conducted on 100 individuals allocated into four groups; 25 healthy controls, 25 patients having OPMDs with dysplasia; 25 patients having OPMDs without dysplasia, and 25 oral cancer patients. Demographic data including data related to different risk factors, modified gingival index, oral hygiene level, in addition to salivary levels of IL-6, IL-8 and sCD44 were assessed.

Detailed Description

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Histopathologic evaluation:

Biopsy samples were obtained from all lesions to verify the diagnosis and establish the presence of dysplasia in the potentially premalignant lesions before allocating patients to their specific groups.

History and clinical assessment:

Demographic data as age and gender, medical history and habits as smoking and alcohol were obtained during patient interview. Modified gingival index (MGI), level of oral hygiene (OH) and the number of remaining natural teeth were also assessed. Subjects not willing to sign a written informed consent, pregnant females, lactating mothers, and patients with immunosuppressive disorders were excluded.

Modified gingival index (MGI) evaluates the presence and degree of gingival inflammation. A score of 0 means absence of inflammation. 1 indicates mild inflammation (slight redness) of any part of the gingiva. 2- mild inflammation of the whole gingiva. 3- moderate inflammation (moderate redness, edema, and/or hypertrophy) of the gingiva. 4-severe inflammation (marked redness and spontaneous bleeding) of the gingiva. Level of OH care was evaluated corresponding to the OH habits of the patient and efficiency of plaque removal. OH, level is scored as: 1- very good, 2- good, 3- fair, and 4- poor OH.

Collection of 1.0-2.0 mL of whole unstimulated saliva was obtained between nine and twelve in the morning, to evade diurnal alteration. Participants refrained from eating, smoking, brushing, and mouthwash use, 2 hours before to salivary sampling, which were stored at -70 ◦C till analyzed.

Quantification of salivary IL-6, IL-8, and sCD44 in all samples using an ELISA kit

List of abbreviations:

OSCC: Oral squamous cell carcinoma OPMDs: Oral potentially malignant disorders HNSCC: Head and neck squamous cell carcinoma MGI: Modified gingival index. OH: Level of oral hygiene ROC: Receiver operating characteristic

Conditions

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Oral Cancer

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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healthy controls

healthy controls

Group Type OTHER

histologic evaluation

Intervention Type DIAGNOSTIC_TEST

histologic evaluation

biochemical analysis

Intervention Type DIAGNOSTIC_TEST

IL-6, IL-8 and sCD44

clinical examination

Intervention Type DIAGNOSTIC_TEST

clinical examination

patients having OPMDs with dysplasia

patients having OPMDs with dysplasia

Group Type OTHER

histologic evaluation

Intervention Type DIAGNOSTIC_TEST

histologic evaluation

biochemical analysis

Intervention Type DIAGNOSTIC_TEST

IL-6, IL-8 and sCD44

clinical examination

Intervention Type DIAGNOSTIC_TEST

clinical examination

patients having OPMDs without dysplasia

patients having OPMDs without dysplasia

Group Type OTHER

histologic evaluation

Intervention Type DIAGNOSTIC_TEST

histologic evaluation

biochemical analysis

Intervention Type DIAGNOSTIC_TEST

IL-6, IL-8 and sCD44

clinical examination

Intervention Type DIAGNOSTIC_TEST

clinical examination

oral cancer patients

oral cancer patients

Group Type OTHER

histologic evaluation

Intervention Type DIAGNOSTIC_TEST

histologic evaluation

biochemical analysis

Intervention Type DIAGNOSTIC_TEST

IL-6, IL-8 and sCD44

clinical examination

Intervention Type DIAGNOSTIC_TEST

clinical examination

Interventions

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histologic evaluation

histologic evaluation

Intervention Type DIAGNOSTIC_TEST

biochemical analysis

IL-6, IL-8 and sCD44

Intervention Type DIAGNOSTIC_TEST

clinical examination

clinical examination

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* patients above 18 years both males and females patients presenting with OPMDs
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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British University In Egypt

OTHER

Sponsor Role lead

Responsible Party

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Dalia Ghalwash

PROFESSOR

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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British University in Egypt

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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BU1612

Identifier Type: -

Identifier Source: org_study_id

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