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Salivary LINC00657 as a Diagnostic Biomarker for Oral Squamous Cell Carcinoma

Salivary LINC00657 as a Diagnostic Biomarker for Oral Squamous Cell Carcinoma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05821179
Enrollment
36
Registered
2023-04-20
Start date
2022-01-01
Completion date
2023-02-25
Last updated
2023-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral Squamous Cell Carcinoma

Keywords

Oral squamous cell carcinoma, oral potentially malignant disorders, saliva, LINC00657, miR-106a.

Brief summary

This study was designed to verify the role of salivary LINC00657 as a diagnostic marker in oral squamous cell carcinoma (OSCC) patients as compared to oral lichen planus (OLP) (as an example of oral potentially malignant lesions) and normal individuals, and to show its relation to miR-106a. A total of 36 participants were included.

Detailed description

This study was designed to verify the role of salivary LINC00657 as a diagnostic marker in oral squamous cell carcinoma (OSCC) patients as compared to oral lichen planus (OLP) (as an example of oral potentially malignant lesions) and normal individuals, and to show its relation to miR-106a. A total of 36 participants were included, subdivided into 3 groups: Group I: 12 patients diagnosed with OSCC. Group II: 12 patients diagnosed with OLP. Group III: 12 systemically free individuals with no oral mucosal lesions. statistical analysis and ROC analysis were performed

Interventions

None listed

Sponsors

Fayoum University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* group I : oral squamous cell carcinoma lesions (OSCC) * group II: oral lichen planus lesions (OLP) * group III: systemically healthy volunteers

Exclusion criteria

* oral lesions other than OSCC / OLP in group I and II * any oral lesion in group III * pregnant females

Design outcomes

Primary

MeasureTime frameDescription
LINC00657 level in salivary samples from all participants measured using PCRlevel of miR-106a is measured after the completion of all salivary sample collection carried at the 1 day of enrollment of subjects in the investigation after diagnosis confirmationquantitative real-time PCR is used to detect LINC00657 levels in saliva samples from patients with OSCC and OPMD compared to healthy subjects

Secondary

MeasureTime frameDescription
miR-106a level in salivary samples from the included subjects evaluated by PCRlevel of miR-106a is measured after the completion of all salivary sample collection carried at the 1 day of enrollment of subjects in the investigationquantitative real-time PCR is used to detect miR106a levels in saliva samples from patients with OSCC and OPMD compared to healthy subjects

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026