ClinicalTrials.Veeva

Menu

Cathelicidin LL-37 Relation to Potentially Malignant Lesions

F

Fayoum University

Status

Completed

Conditions

Oral Potentially Malignant Lesions

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

LL-37 appears to have a potential role in potentially malignant lesions (OLP & leukoplakia). The remarkable diagnostic accuracy of salivary LL-37 in differentiating potentially malignant lesion and healthy control could confirm its utilization as an innovative marker to early diagnose potentially malignant lesions. Salivary LL-37 being non-invasive accurate marker could be as a chair-side diagnostic method that detect potentially malignant lesions.

Full description

Aim: The recognition of practical early diagnostic biomarkers is a cornerstone of improved prevention and treatment of cancer thus the current study estimated salivary level of Cathelicidin LL-37 in patients suffering from potentially malignant lesions and control subjects to corroborate Cathelicidin LL-37 as a diagnostic marker for early detection of potentially malignant diseases and revealing its possible role in carcinogenesis.

Methodology: 45 systemically healthy individuals were subdivided into three groups: Group I: 15 Healthy participants without any oral lesions. Group II: 15 Patients having atrophic/erosive oral lichen planus (OLP). Group III: 15 Patients having oral leukoplakia.. Enzyme linked immune-sorbent assay (ELIZA) kit was used to evaluate the level of LL-37 in whole unstimulated salivary samples collected from all participants. To reveal AUC, sensitivity, specificity, and diagnostic accuracy of LL-37 receiver operating curve (ROC) analysis was done.

Enrollment

45 patients

Sex

All

Ages

30 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Both genders with age range 30 - 70 years.
  • Patients agreed to sign a written consent after understanding the nature of the study.
  • Clinically diagnosed and histologically confirmed as having oral potentially malignant lesions mainly atrophic/erosive oral lichen planus and oral leukoplakia.

Exclusion criteria

  • Systemic diseases as well as pregnant or lactating females.
  • Patients currently taking corticosteroids, immunosuppressives drugs, contraceptive pills, or antibiotics.
  • Patients are diagnosed with any other oral lesions other than oral lichen planus and oral leukoplakia.
  • Vulnerable subjects as prisoners, or mentally disabled.

Trial design

45 participants in 3 patient groups

Group I (control group)
Description:
15 Healthy participants without any oral lesions
Group II:
Description:
15 Patients having atrophic/erosive oral lichen planus (OLP). Group III: 15 Patients having oral leukoplakia
Group III:
Description:
15 Patients having oral leukoplakia

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems