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Melatonin Epigenetic Potential in Preventing Malignant Transformation of Oral Lichen Planus

Melatonin Epigenetic Potential in Preventing Malignant Transformation of Oral Lichen Planus Epigenetic Randomized Clinical Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06533033
Enrollment
50
Registered
2024-08-01
Start date
2024-01-01
Completion date
2024-08-01
Last updated
2024-08-01

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

Conditions

Oral Lichen Planus

Brief summary

Background: Oral Lichen planus (OLP) is one of the most common oral diseases that has an unneglectable rate of malignant transformation. Recently malignant transformation has been definitively linked to epigenetic changes. One of those most common changes is DNA hypermethylation that causes tumor suppressor genes to downtranslate and thus carcinogenesis begins. ZNF582 gene hypermethylation is emerging as an exclusive biomarker to differentiate between normal and dysplastic changes that occur over the epithelium. Aim: To evaluate the Melatonin epigenetic potential in preventing malignant transformation of OLP. Material and methods: an epigenetic randomized clinical study will be conducted on 50 patients suffering from OLP, recruited from the outpatient clinic of Oral medicine department, Alexandria Faculty of Dentistry, Egypt. Patients will be assigned to either Control group who will receive topical corticosteroids and antifungal treatment, or test group who will receive melatonin supplement in addition to conventional treatment. All patients will be genetically evaluated for the level of DNA hypermethylation 8 weeks after treatment, and clinically evaluated for disease severity and pain, by Elsabagh scoring system 4. 8, and 12 weeks after treatment.

Interventions

DRUGRapid Release Capsules Melatoni

Twenty-five will be given melatonin therapy in combination with the conventional treatment. 2 tablets,30 minutes before sleeping once daily for 8 weeks.

DRUGTriamcinolone Acetonide ointment, Kenacort-A orabase

Twenty-five will be given topical corticosteroid applied twice to three times daily. Topical antifungal will be applied three to four times daily. This conventional treatment will be given to the patients for 8 weeks

Sponsors

Hams Hamed Abdelrahman
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients clinically and histopathologically diagnosed to be suffering from OLP in the following forms has been reported in the literature to have the highest potentiality for malignant transformation (plaque-type lichen , Erosive lichen planus, ulcerative lichen planus), with or without histopathological dysplasia. * Patients who have symptoms (i.e. pain and burning sensation) secondary to OLP.

Exclusion criteria

* Patients suspected to have lichenoid drug reaction or lichenoid contact allergy. * Patients suffering from systemic diseases (such as diabetes, cardiovascular or liver disorders, renal dysfunction). * Patients with findings of any physical or mental abnormality that would interfere with or be affected by the study procedure. * Patients who have adverse habits of chewing tobacco and smoking. * Pregnant and lactating women. * Patients under treatment with corticosteroids and immunosuppressants. * Patients exhibiting any skin manifestations of OLP

Design outcomes

Primary

MeasureTime frameDescription
change in DNA methylation level of tumor suppressor gene (ZNF852)up to 8 weeksThe ZNF582 gene sequence will be obtained from the University of California, Santa Cruz, Genomics Institute. website (http://genome.ucsc.edu/), and the methylation-specific PCR primers for ZNF582 will be acquired from MethPrimer (http://www.urogene.org/cgibin/ methprimer/methprimer.cgi).
Change in oral lesionsUp to 12 weeksOral lesions will be evaluated clinically after treatment using Elsabagh et al score. Objective mucosal lesion nature (no lesion= 0, White keratotic lesion =1, Atrophy/Erosion intermixed or not with White lesion = 2, Ulceration intermixed or not with White lesion = 3)
Change in pain scoresUp to 12 weeksSubjective pain score (no pain =0, mild pain=1, moderate pain=2, severe pain=3)
Change in number of affected surfaces in oral cavityUp to 12 weeksNumber of surfaces affected in the oral cavity other than the gingiva (only one surface affected or buccal mucosae bilaterally =0, more than one surface affected or more than both buccal mucosae=1)
Change in gingival involvementUp to 12 weeksGingival involvement as desquamative gingivitis (no gingival involvement = 0, narrow band (1mm) of gingival involvement or wide band in less than 6 teeth involved =1, wide band (\>1mm) of gingival involvement in more than 6 teeth involved = 2)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026