None listed
Conditions
Interventions
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: 1 Adults aged 18?70 years 2 Histologically confirmed OPLs (e.g.leukoplakia, oral epithelial dysplasia) 3 Lesion size should be more than or equal to 1cm 4 No prior treatment for the current lesion. 5 Willingness to comply with study procedures and provide informed consent.
Exclusion criteria
Exclusion criteria: 1 Malignant oral lesions 2 Severe systemic conditions or immunocompromised status 3 Pregnancy or lactation 4 Known hypersensitivity to resveratrol 5 Concurrent use of other chemopreventive agents.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ? Change in lesion size and clinical appearance. ? Histopathological assessment of dysplasia grade. Timepoint: Duration of study - 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| ? Patient-reported pain & discomfort scores. ? Incidence of adverse events. ? Biomarker analysis for molecular mechanismsTimepoint: Duration of study -12 months | — |
Countries
India
Contacts
Manav rachna dental college