Validation of Salivary Proteomic Biomarkers for Early Detection of Oral Cancer in Egyptian Population
NCT ID: NCT06471270
Last Updated: 2024-06-24
Study Results
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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COMPLETED
NA
100 participants
INTERVENTIONAL
2023-07-15
2024-03-15
Brief Summary
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Detailed Description
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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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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Study Groups
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healthy controls
healthy controls
histologic evaluation
histologic evaluation
biochemical analysis
IL-6, IL-8 and sCD44
clinical examination
clinical examination
patients having OPMDs with dysplasia
patients having OPMDs with dysplasia
histologic evaluation
histologic evaluation
biochemical analysis
IL-6, IL-8 and sCD44
clinical examination
clinical examination
patients having OPMDs without dysplasia
patients having OPMDs without dysplasia
histologic evaluation
histologic evaluation
biochemical analysis
IL-6, IL-8 and sCD44
clinical examination
clinical examination
oral cancer patients
oral cancer patients
histologic evaluation
histologic evaluation
biochemical analysis
IL-6, IL-8 and sCD44
clinical examination
clinical examination
Interventions
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histologic evaluation
histologic evaluation
biochemical analysis
IL-6, IL-8 and sCD44
clinical examination
clinical examination
Eligibility Criteria
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Inclusion Criteria
18 Years
70 Years
ALL
Yes
Sponsors
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British University In Egypt
OTHER
Responsible Party
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Dalia Ghalwash
PROFESSOR
Locations
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British University in Egypt
Cairo, , Egypt
Countries
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Other Identifiers
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BU1612
Identifier Type: -
Identifier Source: org_study_id
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